MEDLINE procedure kits labeled as follows recallZ-0509-2025 · MEDLINE INDUSTRIES, LP - Northfield · initiated Oct 16, 2024
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
FDA root cause category: Under Investigation by firm
What the company is doing
An IMMEDIATE ACTION REQUIRED RECALL notification letter dated 10/16/24 was sent to customers. REQUIRED ACTION: 1.Immediately check your stock for the affected item number and the affected lot numbers which can be located within the recall portal. Quarantine all affected product immediately. 2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form. 3.Upon receipt of your submitted response form, your account will receive over-labels to place unaffected inventory, with instructions for your staff to remove the affected component prior to using the kit. These labels will be provided via FedEx overnight, if applicable. The login for completing the response form is: Website link: https://recalls.medline.comRecall Reference #: R-24-216-FGRecall Code: 4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].
Recall details
- Recall number
- Z-0509-2025
- Status
- Open, Classified
- Initiated by the company
- Oct 16, 2024
- Posted by the FDA
- Nov 22, 2024
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Product code
- OFT
- Distribution
- US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands
Product description
MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268B; 2) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268C; 3) FEMORAL BLOCK TRAY, REF DYNJRA1739A; 4) FEMORAL BLOCK TRAY, REF DYNJRA1739B; 5) 18G CPNB 20G STYLETED CATHETER, REF DYNJRA1869; 6) CONT EPID 18G NDL/20G CATH, REF DYNJRA9035; 7) TRAY 18G CPNB 20G STYLETED, REF DYNJRA9040; 8) CATHETER REINF W/ CONNECT OT, REF EPIREINF19O; 9) CATHETER REINF WITH CONNECTOR, REF EPIREINF29C; 10) CONTINUOUS EPIDURAL UPDATED, REF PAIN0384B; 11) CONT EPI 20G W/HUSTEAD, REF PAIN1069C; 12) CONTINUOUS EPIDURAL, REF PAIN1271A; 13) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN1281B; 14) CONTINUOUS EPIDURAL TRAY, REF PAIN1317; 15) 20G CONT. EPID TRAY, REF PAIN1353B; 16) CONTINUOUS EPIDURAL TRAY, REF PAIN1358; 17) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN1361; 18) JHAC CONT EPIDURAL, REF PAIN1437A; 19) CONTINUOUS EPIDURAL TRAY, REF PAIN1453B; 20) EPIDURAL CATH KIT, REF PAIN1536A; 21) CONTINUOUS EPIDURAL TRAY, REF PAIN1547; 22) EPIDURAL TRAY, REF PAIN1558; 23) CONTINUOUS EPIDURAL, REF PAIN1581A; 24) CONTINUOUS EPIDURAL TRAY, REF PAIN1587A; 25) CONTINUOUS EPIDURAL TRAY, REF PAIN1587B; 26) CONTINUOUS EPIDURAL TRAY, REF PAIN1605A; 27) CONTINUOUS EPIDURAL TRAY, REF PAIN1636; 28) EPIDURAL CATHETERIZATION KIT, REF PAIN1644A; 29) CONTINUOUS EPIDURAL TRAY, REF PAIN1667A; 30) CONT. EPIDURAL TRAY - NYLON, REF PAIN1709; 31) CONT. EPIDURAL TRAY - NYLON, REF PAIN1709A; 32) CONTINUOUS EPIDURAL, REF PAIN1766A; 33) PEDIATRIC EPIDURAL TRAY, REF PAIN1806; 34) EPIDURAL TRAY IMF 103130, REF PAIN1807; 35) CONTINUOUS EPIDURAL TRAY, REF PAIN1816; 36) CONTINUOUS EPIDURAL, REF PAIN1844; 37) CSE TRAY, REF PAIN1845; 38) BWH L&D EPIDURAL KIT, REF PAIN1846; 39) 17G CONT. EPI - MRI SAFE, REF PAIN1854; 40) 17G L&D CONT. EPIDURAL, REF PAIN1855; 41) CONTINUOUS/CSE TRAY, REF PAIN1856; 42) CONTINUOUS/CSE TRAY, REF PAIN1856A; 43) CONTINUOUS EPIDURAL TRAY, REF PAIN1864; 44) CONTINUOUS EPIDURAL TRAY, REF PAIN1864A; 45) CONTINUOUS EPIDURAL TRAY, REF PAIN1878; 46) CSE TRAY, REF PAIN1885; 47) TEAM HEALTH EPIDURAL, REF PAIN1887; 48) SOUND ANESTHESIA EPIDURAL, REF PAIN1888; 49) CONTINUOUS EPIDURAL TRAY, REF PAIN1890; 50) CONTINUOUS EPIDURAL TRAY, REF PAIN1892; 51) UAMS CONTINUOUS EPIDURAL, REF PAIN1893; 52) TRAY,CON,EPID,19G REINF,W/TUOH, REF PAIN1894; 53) CSE TRAY, REF PAIN1898; 54) CSE TRAY, REF PAIN1904; 55) 17/25G CSE TRAY, REF PAIN1919; 56) CSE TRAY, REF PAIN1920; 57) 17/25G CSE TRAY, REF PAIN1937; 58) CONTINUOUS EPIDURAL TRAY, REF PAIN1940; 59) COMBINED SPINAL EPIDURAL TRAY, REF PAIN1958; 60) REINFORCED CATH EPIDURAL TRAY, REF PAIN1967; 61) OPEN TIP EPIDURAL CATH TRAY, REF PAIN2014; 62) TRAY,CON,EPID,19G REINF,W/TUOH, REF PAIN9025; 63) TRAY,CON,EPID,19G REINF,W/O RX, REF PAIN9026; 64) CSE 17G HUSTEAD 27G WHIT W/RX, REF PAIN9028; 65) 17G CONT EPIDURAL NYLON, REF PAIN9030; 66) TRAY,CON EPID,19G REINF OPNTIP, REF PAIN9031; 67) 19G REINF CATH LIDO/NACL ONLY, REF PAIN9034; 68) 20G NYLON CATH LIDO/NACL ONLY, REF PAIN9035; 69) 17GHUST 27GWHIT LIDO/NACL ONLY, REF PAIN9036; 70) REINIF 19G EPI CATH S STERILE, REF REPICATH19; 71) CONT. EPIDURAL TRAY, REF SAMPA0105; 72) EPIDURAL CATH PACK, REF SAMPA0106; 73) CONTINUOUS EPIDURAL TRAY, REF SAMPA0110; 74) CONTINUOUS EPIDURAL TRAY, REF SAMPA0111
Code information (models, lots, serial numbers)
Show the full code information (9k characters)
Codes: 1) DYNJRA1268B, UDI/DI 10193489370485 (each) 40193489370486 (case), Lot Numbers: 20FLA512, 20HLA422, 20ILA296, 20ILA327, 20LLA223, 21ALA087, 21CLA525; 2) DYNJRA1268C, UDI/DI 10193489905830 (each) 40193489905831 (case), Lot Numbers: 21ELA224, 21ELA333, 21GLA292, 21GLA895, 21HLA924, 21ILA773, 21JLA824, 22ALA237, 22BLA899, 22DLA197, 22DLA409, 22ELA583, 22ELB120, 22FLA820, 22FLB163, 22GLB081, 22HLA566, 22ILA092, 22LLA800, 23DLA368, 23FLA942, 23GLA321, 23HLA910, 23ILA593, 23JLA268; 3) DYNJRA1739A, UDI/DI 1019348992495 (each) 40193489924955 (case), Lot Numbers: 23CBE392; 4) DYNJRA1739B, UDI/DI 10195327411237 (each) 40195327411238 (case), Lot Numbers: 23FBL394, 23GBV201, 23HBG282, 23HBG968, 23IBQ191; 5) DYNJRA1869, UDI/DI 10195327018818 (each) 40195327018819 (case), Lot Numbers: 23CBE391; 6) DYNJRA9035, UDI/DI 10884389618448 (each) 40884389618449 (case), Lot Numbers: 22GBO435, 22IBI073, 23BBB167, 23BBS677, 23CBL304, 23FBI382; 7) DYNJRA9040, UDI/DI 10193489830514 (each) 40193489830515 (case), Lot Numbers: 23CBO446, 23DBK742, 23HBG091, 23HBG092; 8) EPIREINF19O, UDI/DI 10195327222970 (each) 40195327222971 (case), Lot Numbers: 22HBB281, 23EBO266, 23GBA230, 23HBN806, 23HBR131, 23HBY420; 9) EPIREINF29C, UDI/DI 10195327114367 (each) 40195327114368 (case), Lot Numbers: 22FBU886, 22HBD608, 22KBK655, 22NBE738, 23ABH589, 23DBK772, 23DBN448, 23JBU253; 10) PAIN0384B, UDI/DI 10193489926842 (each) 40193489926843 (case), Lot Numbers: 23BMC466, 23FMJ516, 23FMJ523, 23FMJ721, 23HMA617, 23LMB080, 23LMC430; 11) PAIN1069C, UDI/DI 1019532736489 (each) 40195327364893 (case), Lot Numbers: 23ELA637, 23GLA586, 23HLA616, 23JLB208; 12) PAIN1271A, UDI/DI 10193489619201 (each) 40193489619202 (case), Lot Numbers: 23BLA979; 13) PAIN1281B, UDI/DI 10195327288211 (each) 40195327288212 (case), Lot Numbers: 22KLA735, 23ALA157; 14) PAIN1317, UDI/DI 10888277797109 (each) 40888277797100 (case), Lot Numbers: 22GLA179, 22HLB332, 23CLA460, 23DLA279, 23ELB138, 23FLA944, 23GLA948, 23HLB106, 23ILA924, 23JLB213, 23KLB167; 15) PAIN1353B, UDI/DI 10193489336726 (each) 40193489336727 (case), Lot Numbers: 20ELA452; 16) PAIN1358, UDI/DI 10193489586749 (each) 40193489586740 (case), Lot Numbers: 22FLB088, 23CLA573; 17) PAIN1361, UDI/DI 10193489586848 (each) 40193489586849 (case), Lot Numbers: 22FLA642, 22GLA243, 23ILA612, 23JLA051; 18) PAIN1437A, UDI/DI 1019532713519 (each) 40195327135196 (case), Lot Numbers: 22EBA985, 23ABO995, 23KBH798, 23KBR650; 19) PAIN1453B, UDI/DI 1019532731038 (each) 40195327310388 (case), Lot Numbers: 22LLB007, 23ALA593, 23BLA987; 20) PAIN1536A, UDI/DI 10193489288582 (each) 40193489288583 (case), Lot Numbers: 23CLA081; 21) PAIN1547, UDI/DI 10193489813081 (each) 40193489813082 (case), Lot Numbers: 23BLB100, 23FLA069, 23JLA884; 22) PAIN1558, UDI/DI 10193489213584 (each) 40193489213585 (case), Lot Numbers: 23BMH883, 23GMA342, 23GMC058, 23IMC928; 23) PAIN1581A, UDI/DI 10195327351809 (each) 40195327351800 (case), Lot Numbers: 23BLB024, 23CLA024, 23ELB140; 24) PAIN1587A, UDI/DI 10193489336368 (each) 40193489336369 (case), Lot Numbers: 23BLA078, 23FLA277; 25) PAIN1587B, UDI/DI 10195327539511 (each) 40195327539512 (case), Lot Numbers: 23JLB184; 26) PAIN1605A, UDI/DI 1019348946814 (each) 40193489468145 (case), Lot Numbers: 22KLA748, 23BLA153; 27) PAIN1636, UDI/DI 10193489312720 (each) 40193489312721 (case), Lot Numbers: 22FLA297; 28) PAIN1644A, UDI/DI 10195327427863 (each) 40195327427864 (case), Lot Numbers: 23GLA589, 23HLA915, 23JLA225, 23KLA831; 29) PAIN1667A, UDI/DI 10193489472868 (each) 40193489472869 (case), Lot Numbers: 22FLB089, 23CLA442, 23ELA958, 23FLA945, 23HLA916, 23KLB169; 30) PAIN1709, UDI/DI 10193489816044 (each) 40193489816045 (case), Lot Numbers: 23CLA719; 31) PAIN1709A, UDI/DI 10195327411220 (each) 40195327411221 (case), Lot Numbers: 23ELA723, 23ILA927; 32) PAIN1766A, UDI/DI 10195327361488 (each) 40195327361489 (case), Lot Numbers: 23FLB123, 23GLA313; 33) PAIN1806, UDI/DI 10195327134563 (each) 40195327134564 (case), Lot Numbers: 22ELA290, 22FLB111; 34) PAIN1807, UDI/DI 1019532713502 (each) 40195327135028 (case), Lot Numbers: 22FLB112, 23DLA445; 35) PAIN1816, UDI/DI 10195327145453 (each) 40195327145454 (case), Lot Numbers: 22GLA509, 22GLA531; 36) PAIN1844, UDI/DI 10195327207748 (each) 40195327207749 (case), Lot Numbers: 23BLA981, 23ELB126, 23ILA404, 23ILB016; 37) PAIN1845, UDI/DI 10195327210823 (each) 40195327210824 (case), Lot Numbers: 23ELA640; 38) PAIN1846, UDI/DI 10195327211639 (each) 40195327211630 (case), Lot Numbers: 23DLA446; 39) PAIN1854, UDI/DI 10195327225858 (each) 40195327225859 (case), Lot Numbers: 22JLB193, 22LLA402; 40) PAIN1855, UDI/DI 10195327226015 (each) 40195327226016 (case), Lot Numbers: 22LLA455, 23CLA867; 41) PAIN1856, UDI/DI 10195327228996 (each) 40195327228997 (case), Lot Numbers: 22JLB162, 22LLA409; 42) PAIN1856A, UDI/DI 10195327338015 (each) 40195327338016 (case), Lot Numbers: 23HLB303; 43) PAIN1864, UDI/DI 10195327238766 (each) 40195327238767 (case), Lot Numbers: 22HLB077, 22LLA731, 23FLA012; 44) PAIN1864A, UDI/DI 10195327517090 (each) 40195327517091 (case), Lot Numbers: 23LLA277; 45) PAIN1878, UDI/DI 10195327257842 (each) 40195327257843 (case), Lot Numbers: 23ALA348, 23ELA724; 46) PAIN1885, UDI/DI 10195327269159 (each) 40195327269150 (case), Lot Numbers: 22LLA664, 23DLA281, 23ELA641; 47) PAIN1887, UDI/DI 10195327272852 (each) 40195327272853 (case), Lot Numbers: 22KLA920; 48) PAIN1888, UDI/DI 10195327272913 (each) 40195327272914 (case), Lot Numbers: 23BLA151, 23BLB105; 49) PAIN1890, UDI/DI 10195327282387 (each) 40195327282388 (case), Lot Numbers: 23BLB106; 50) PAIN1892, UDI/DI 10195327283049 (each) 40195327283040 (case), Lot Numbers: 23BLB026, 23ELB077, 23ILA928; 51) PAIN1893, UDI/DI 10195327283865 (each) 40195327283866 (case), Lot Numbers: 23BLA283, 23GLA624, 23HLA803; 52) PAIN1894, UDI/DI 10195327283896 (each) 40195327283897 (case), Lot Numbers: 23BLB107, 23ELA725, 23GLA370; 53) PAIN1898, UDI/DI 10195327297596 (each) 40195327297597 (case), Lot Numbers: 23BLA284, 23BLA726; 54) PAIN1904, UDI/DI 10195327312336 (each) 40195327312337 (case), Lot Numbers: 23ELB079, 23GLA947, 23HLA774; 55) PAIN1919, UDI/DI 10195327342807 (each) 40195327342808 (case), Lot Numbers: 23CLA461, 23GLB137, 23HLA653, 23ILA462; 56) PAIN1920, UDI/DI 10195327346072 (each) 40195327346073 (case), Lot Numbers: 23FLA827, 23HLA259; 57) PAIN1937, UDI/DI 10195327362737 (each) 40195327362738 (case), Lot Numbers: 23ELB122; 58) PAIN1940, UDI/DI 10195327365332 (each) 40195327365333 (case), Lot Numbers: 23ELB080; 59) PAIN1958, UDI/DI 10195327399986 (each) 40195327399987 (case), Lot Numbers: 23GBV335, 23IBL615; 60) PAIN1967, UDI/DI 10195327417482 (each) 40195327417483 (case), Lot Numbers: 23IDA109, 23KDB373; 61) PAIN2014, UDI/DI 10195327510763 (each) 40195327510764 (case), Lot Numbers: 23JBS142; 62) PAIN9025, UDI/DI 10193489777697 (each) 40193489777698 (case), Lot Numbers: 22FLB008, 22LLA741; 63) PAIN9026, UDI/DI 10193489777703 (each) 40193489777704 (case), Lot Numbers: 23ALA479, 23ALA534, 23ALA753, 23BLA647, 23BLB091, 23CLA295; 64) PAIN9028, UDI/DI 10193489295689 (each) 40193489295680 (case), Lot Numbers: 22GLA287, 22ILA124, 23CLA410; 65) PAIN9030, UDI/DI 10193489295641 (each) 40193489295642 (case), Lot Numbers: 22FLB009, 22HLB347, 22ILA078, 23CLA407; 66) PAIN9031, UDI/DI 10195327146429 (each) 40195327146420 (case), Lot Numbers: 22GLA057, 23ALA831, 23ELA887, 23GLA871; 67) PAIN9034, UDI/DI 10195327287757 (each) 40195327287758 (case), Lot Numbers: 23ABB439, 23ABG209, 23BBS341, 23CBO460, 23EBM262, 23EBR039, 23FBI376, 23FBI377; 68) PAIN9035, UDI/DI 10195327288006 (each) 40195327288007 (case), Lot Numbers: 23BBP889; 69) PAIN9036, UDI/DI 10195327288013 (each) 40195327288014 (case), Lot Numbers: 23BBN205, 23GBW665, 23HBQ304, 23HBU314, 23JBO472; 70) REPICATH19, UDI/DI 10193489630848 (each) 40193489630849 (case), Lot Numbers: 22ABM967, 22GBG329, 22HBO372, 23CBI450, 23GBI168, 23GBI169, 23GBI170, 23HBI971; 71) SAMPA0105, UDI/DI 10195327026240 (each) 40195327026241 (case), Lot Numbers: 21JLA580; 72) SAMPA0106, UDI/DI 10195327028169 (each) 40195327028160 (case), Lot Numbers: 21LBY057; 73) SAMPA0110, UDI/DI 10195327097004 (each) 40195327097005 (case), Lot Numbers: 22BLA107, 22CLA719, 22CLA850; 74) SAMPA0111, UDI/DI 10195327204693 (each) 40195327204694 (case), Lot Numbers: 22LLA665
Devices named in this recall
73 devices in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNJRA9040Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls2 reports
- Medline Industries, Inc. DYNJRA1739AMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1869Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1739BMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. PAIN1317Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. PAIN1667AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall4 reports
- Medline Industries, Inc. DYNJRA1268CMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall4 reports
- Medline Industries, Inc. PAIN9028Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall2 reports
- Medline Industries, Inc. PAIN9025Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall2 reports
- Medline Industries, Inc. PAIN1894Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall2 reports
- Medline Industries, Inc. PAIN1587AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall1 report
- Medline Industries, Inc. PAIN9031Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall1 report
- Medline Industries, Inc. PAIN1855Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall1 report
- Medline Industries, Inc. PAIN1919Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall1 report
- Medline Industries, Inc. PAIN1558Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1536AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN9030Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1636Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1353BMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. DYNJRA1268BMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1605AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1358Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1361Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1271AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN9026Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1547Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1709Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN0384BMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. SAMPA0105Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. SAMPA0106Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. SAMPA0110Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. EPIREINF29CMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1806Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1807Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1437AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1816Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. SAMPA0111Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1844Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1845Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1846Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. EPIREINF19OMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1854Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1856Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1864Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1878Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1885Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1887Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1888Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1890Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1892Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1893Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN9034Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN9035Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN9036Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1281BMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1898Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1453BMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1904Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1856AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1920Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1581AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1766AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1937Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1069CMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1940Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1958Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1709AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1967Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1644AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN2014Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1864AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. PAIN1587BMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
- Medline Industries, Inc. DYNJRA9035Medline Industries, Inc. · Spinal epidural anesthesia kit1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 95615).
- Z-0508-2025 · Open, ClassifiedMEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
- Z-0510-2025 · Open, ClassifiedMEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20
- Z-0511-2025 · Open, ClassifiedMEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A
- Z-0512-2025 · Open, ClassifiedMEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) EPIDURAL CATHETERIZATION KIT, REF P…
- Z-0513-2025 · Open, ClassifiedMEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON EPID 20G NYL W/TUOHY, REF PAIN9023; 4) TRAY, CONT EPI 2…
- Z-0514-2025 · Open, ClassifiedMEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
- Z-0515-2025 · Open, ClassifiedMEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699A
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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