MEDLINE convenience kits labeled as recallZ-0513-2026 · Medline Industries, LP · initiated Sep 30, 2025
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 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
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.
FDA root cause category: Under Investigation by firm
What the company is doing
Medline issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 09/30/2025 and 10/6/2025 via email and mail. The notice explained the issue with the component, potential risk, and requested the following actions: 1. Immediately check stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. 2. Please use the link and the information found in the notice to complete the response form. Please list the quantity of affected product in inventory on the form. Even if no affected product is in inventory, please complete and submit the form. 3. Upon receipt of the submitted response form, the customer account will receive over-labels to place on affected inventory, with instructions for the customer staff to remove and discard the affected component prior to using the kit. These labels will be provided via FedEx overnight, if applicable. 4. For distributors or those who have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please include your customers quantities on your response form. Upon receipt of your submitted response form, you will receive over-labels to provide to your customers to affix to their affected product. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].
Recall details
- Recall number
- Z-0513-2026
- Status
- Open, Classified
- Initiated by the company
- Sep 30, 2025
- Posted by the FDA
- Nov 14, 2025
- Recalling firm
- Medline Industries, LP
- Quantity
- 5133 kits
- Product code
- OEZ
- Distribution
- US Nationwide distribution.
Product description
MEDLINE convenience kits labeled as: 1) GENERAL AAA #11-RF, REF CDS840261AB; 2) CAROTID ENDARTERECTOMY CDS-LF, REF CDS983637I; 3) PERIPHERAL VASCULAR CDS, REF CDS983723J; 4) ACH OPEN HEART, REF CDS983773J; 5) VASCULAR, REF CDS984255K; 6) OPEN HEART CHILDRENS PACK-LF, REF DYNJ0161262C; 7) VASCULAR PACK-LF, REF DYNJ0421380P; 8) GEN FEM POP #14-RF, REF DYNJ21877W; 9) VASCULAR PACK, REF DYNJ22350L; 10) GENERAL CAROTID/AV TRAY #15-RF, REF DYNJ27432AC; 11) OPEN HEART PACK, REF DYNJ37284K; 12) ACH CABG ADD-ON, REF DYNJ38175L; 13) CARDIOVASCULAR PACK, REF DYNJ42921G; 14) CABG PACK-LF, REF DYNJ43207K; 15) HEART DRAPING PACK-LF, REF DYNJ43214F; 16) AAA PACK, REF DYNJ44847I; 17) CASTRO CABG-COMPONENT PACK, REF DYNJ44857U; 18) FISTULA PACK, REF DYNJ44869K; 19) MAJOR VASCULAR LEG-TEAM, REF DYNJ44879K; 20) PERMANENT PACING, REF DYNJ44886M; 21) CAROTID VASCULAR ENDARTERECTMY, REF DYNJ50528M; 22) DR DANIELSON AC PACK, REF DYNJ51038R; 23) VASCULAR CAROTID PACK, REF DYNJ56838F; 24) VASCULAR FEM PACK, REF DYNJ56839D; 25) PK CUST OPEN HEART A AND B, REF DYNJ60548B; 26) PK CUST CAROTID ST MICHAE, REF DYNJ60783B; 27) CAROTID PACK, REF DYNJ61659A; 28) VASCULAR MINOR PACK, REF DYNJ62097C; 29) VASCULAR PACK-LF, REF DYNJ65039C; 30) PACEMAKER PACK, REF DYNJ66033B; 31) DR MELLINGER AC PACK, REF DYNJ80609D; 32) HEART PACK II, REF DYNJ81581B; 33) AV FISTULA PACK, REF DYNJ81605; 34) MAJOR VASCULAR PACK, REF DYNJ81610B; 35) CABG ACCESSORY PACK, REF DYNJ82166; 36) VALVE ACCESSORY PACK, REF DYNJ82217; 37) PERIVASCULAR CUSTOM PACK, REF DYNJ84017B; 38) CAROTID ENDARTERECTOMY PACK-LF, REF DYNJ85109; 39) ACH OPEN HEART A&B PK, REF DYNJ85110; 40) VASCULAR ABDOMINAL PACK, REF DYNJ85118; 41) AV FISTULA PACK-LF, REF DYNJ85121; 42) CARDIAC - DEEIK PACK, REF DYNJ85637; 43) VASCULAR, REF DYNJ900293K; 44) VASCULAR-LF, REF DYNJ900714C; 45) HEART/MAJOR VASCULAR, REF DYNJ901066K; 46) MODULE OPEN HEART, REF DYNJ903042P; 47) VASCULAR/OR ANGIO, REF DYNJ905079F; 48) OPEN HEART, REF DYNJ905497B; 49) AAA, REF DYNJ906175B; 50) VASCULAR ABDOMINAL, REF DYNJ907105D; 51) CV COMPLETE, REF DYNJ907904A; 52) KIT CV NURSE CENTRAL DUPAGE, REF DYNJ908820; 53) KIT CV NURSE CENTRAL DUPAGE, REF DYNJ908820A.
Code information (models, lots, serial numbers)
Show the full code information (6k characters)
1) CDS840261AB: UDI/DI 10195327104535 (each), 40195327104536 (case), Lot Numbers: 23FBF165, 23JBM632. 2) CDS983637I: UDI/DI 10195327228125 (each), 40195327228126 (case), Lot Numbers: 23GBU191. 3) CDS983723J: UDI/DI 10195327327828 (each), 40195327327829 (case), Lot Numbers: 23FBA013, 23FBH486, 23GBE805. 4) CDS983773J: UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Numbers: 23GBT133, 23HBH924, 23HBL135, 23HBV936. 5) CDS984255K: UDI/DI 10193489288605 (each), 40193489288606 (case), Lot Numbers: 23KBU348, 24ABB883, 24ABS338. 6) DYNJ0161262C: UDI/DI 10195327357283 (each), 40195327357284 (case), Lot Numbers: 23GDB197, 23GDB757. 7) DYNJ0421380P: UDI/DI 10195327084271 (each), 40195327084272 (case), Lot Numbers: 23DMI590, 23FMJ656. 8) DYNJ21877W: UDI/DI 10195327104542 (each), 40195327104543 (case), Lot Numbers: 23FBT682, 23GBF898, 23IBC645, 24ABR316. 9) DYNJ22350L: UDI/DI 10193489445251 (each), 40193489445252 (case), Lot Numbers: 23LBU055, 24BBQ300. 10) DYNJ27432AC: UDI/DI 10195327104511 (each), 40195327104512 (case), Lot Numbers: 23EBU150, 23GBF873, 23HBQ650, 23IBB637. 11) DYNJ37284K: UDI/DI 10195327401030 (each), 40195327401031 (case), Lot Numbers: 23IBP124, 23KBF938, 24ABS487. 12) DYNJ38175L: UDI/DI 10195327227906 (each), 40195327227907 (case), Lot Numbers: 23FLA915, 23ILA168. 13) DYNJ42921G: UDI/DI 10193489981384 (each), 40193489981385 (case), Lot Numbers: 23FBU282, 23IBT172. 14) DYNJ43207K: UDI/DI 10193489952926 (each), 40193489952927 (case), Lot Numbers: 23EME962. 15) DYNJ43214F: UDI/DI 10193489953077 (each), 40193489953078 (case), Lot Numbers: 23EMA158. 16) DYNJ44847I: UDI/DI 10195327127558 (each), 40195327127559 (case), Lot Numbers: 23HLA758, 23HLB101, 23LLA759. 17) DYNJ44857U: UDI/DI 10195327298067 (each), 40195327298068 (case), Lot Numbers: 23GBI967, 23GBQ950. 18) DYNJ44869K: UDI/DI 10195327127657 (each), 40195327127658 (case), Lot Numbers: 23GBI967, 23GBQ950, 23KMC104. 19) DYNJ44879K: UDI/DI 10195327282233 (each), 40195327282234 (case), Lot Numbers: 23DBI854, 23EBH319, 23GBT541. 20) DYNJ44886M: UDI/DI 10195327127749 (each), 40195327127740 (case), Lot Numbers: 23DBN895, 23EBU129, 23FBQ134, 23GBQ953, 23HBT951. 21) DYNJ50528M: UDI/DI 10195327129699 (each), 40195327129690 (case), Lot Numbers: 23EBA780, 23EBS770, 23GBT274. 22) DYNJ51038R: UDI/DI 10195327298258 (each), 40195327298259 (case), Lot Numbers: 23HBD834. 23) DYNJ56838F: UDI/DI 10195327277857 (each), 40195327277858 (case), Lot Numbers: 23GDA228, 23HDA839. 24) DYNJ56839D: UDI/DI 10195327277864 (each), 40195327277865 (case), Lot Numbers: 23GDA320. 25) DYNJ60548B: UDI/DI 10195327361761 (each), 40195327361762 (case), Lot Numbers: 23EBD777, 23IBS545, 23JBJ740. 26) DYNJ60783B: UDI/DI 10195327361846 (each), 40195327361847 (case), Lot Numbers : 23EBR616, 23GBW384, 23IBV398. 27) DYNJ61659A: UDI/DI 10193489929638 (each), 40193489929639 (case), Lot Numbers: 23HBI627. 28) DYNJ62097C: UDI/DI 10195327189839 (each), 40195327189830 (case), Lot Numbers: 23DBJ117, 23EBD473, 23HBQ663, 23IBB641. 29) DYNJ65039C: UDI/DI 10195327528256 (each), 40195327528257 (case), Lot Numbers: 24BMF955, 24CMB409, 24CME382, 24FMH176. 30) DYNJ66033B: UDI/DI 10195327680589 (each), 40195327680580 (case), Lot Numbers: 24EBA176. 31) DYNJ80609D: UDI/DI 10195327298296 (each), 40195327298297 (case), Lot Numbers: 23HBR318, 23HBZ183. 32) DYNJ81581B: UDI/DI 10195327379254 (each), 40195327379255 (case), Lot Numbers: 23EBO537, 23GBQ499, 23HBG425. 33) DYNJ81605: UDI/DI 10195327123888 (each), 40195327123889 (case), Lot Numbers: 23DBL829, 23EBI374, 23EBM656. 34) DYNJ81610B: UDI/DI 10195327398316 (each), 40195327398317 (case), Lot Numbers: 23EBA748, 23IBP506. 35) DYNJ82166: UDI/DI 10195327182564 (each), 40195327182565 (case), Lot Numbers: 23FDA955. 36) DYNJ82217: UDI/DI 10195327183585 (each), 40195327183586 (case), Lot Numbers: 23DDB931, 23HDA667. 37) DYNJ84017B: UDI/DI 10198459253089 (each), 40198459253080 (case), Lot Numbers: 25CMF132. 38) DYNJ85109: UDI/DI 10195327460594 (each), 40195327460595 (case), Lot Numbers: 23JBD986. 39) DYNJ85110: UDI/DI 10195327460792 (each), 40195327460793 (case), Lot Numbers: 23KBF140. 40) DYNJ85118: UDI/DI 10195327460730 (each), 40195327460731 (case), Lot Numbers: 23KBI277. 41) DYNJ85121: UDI/DI 10195327460853 (each), 40195327460854 (case), Lot Numbers: 23IBR236, 23JBC564. 42) DYNJ85637: UDI/DI 10195327528188 (each), 40195327528189 (case), Lot Numbers: 24CBL150. 43) DYNJ900293K: UDI/DI 10195327554064 (each), 40195327554065 (case), Lot Numbers: 24ABE610, 24BBT270, 24DBU219. 44) DYNJ900714C: UDI/DI 10193489951363 (each), 40193489951364 (case), Lot Numbers: 23FBL767, 23HBW562, 23JBF697. 45) DYNJ901066K: UDI/DI 10195327239282 (each), 40195327239283 (case), Lot Numbers: 23HBB464, 23HBC020, 23JBF553, 23JBW634. 46) DYNJ903042P: UDI/DI 10195327438388 (each), 40195327438389 (case), Lot Numbers: 23JBL424, 23LBL094, 24ABS138. 47) DYNJ905079F: UDI/DI 10195327209001 (each), 40195327209002 (case), Lot Numbers: 23GBV464, 23HBO354. 48) DYNJ905497B: UDI/DI 10193489951639 (each), 40193489951630 (case), Lot Numbers: 23GBB505, 23HBN192, 23JBV542, 23JBV684. 49) DYNJ906175B: UDI/DI 10195327480127 (each), 40195327480128 (case), Lot Numbers: 24FMI570. 50) DYNJ907105D: UDI/DI 10195327233624 (each), 40195327233625 (case), Lot Numbers: 23EBG144, 23EBT013, 23FBI805, 23FBQ992. 51) DYNJ907904A: UDI/DI 10193489992434 (each), 40193489992435 (case), Lot Numbers: 23JME513, 23KMD522. 52) DYNJ908820: UDI/DI 10195327185671 (each), 40195327185672 (case), Lot Numbers: 23JMG465, 23KMI460. 53) DYNJ908820A: UDI/DI 10195327546045 (each), 40195327546046 (case), Lot Numbers: 23LMH559, 24CMA145, 24DMF994, 24DMI666.
Devices named in this recall
53 devices in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNJ51038RMedline Industries, Inc. · Cardiovascular procedure kit4 recalls2 reports
- Medline Industries, Inc. DYNJ42921GMedline Industries, Inc. · Cardiovascular procedure kit4 recalls0 reports
- Medline Industries, Inc. CDS840261ABMedline Industries, Inc. · Cardiovascular procedure kit4 recalls0 reports
- Medline Industries, Inc. DYNJ905079FMedline Industries, Inc. · Cardiovascular procedure kit4 recalls0 reports
- Medline Industries, Inc. CDS983773JMedline Industries, Inc. · Cardiovascular procedure kit4 recalls0 reports
- Medline Industries, Inc. DYNJ81610BMedline Industries, Inc. · Cardiovascular procedure kit4 recalls0 reports
- Medline Industries, Inc. DYNJ903042PMedline Industries, Inc. · Cardiovascular procedure kit3 recalls1 report
- Medline Industries, Inc. DYNJ22350LMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ900714CMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ905497BMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ21877WMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ81605Medline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ50528MMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. CDS983637IMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ56838FMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ44857UMedline Industries, Inc. · Cardiovascular procedure kit3 recalls0 reports
- Medline Industries, Inc. DYNJ62097CMedline Industries, Inc. · Cardiovascular procedure kit2 recalls1 report
- Medline Industries, Inc. CDS984255KMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ61659AMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ43207KMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ43214FMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ907904AMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ0421380PMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ27432ACMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ44847IMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ44869KMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ44886MMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ82166Medline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ82217Medline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ908820Medline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ38175LMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ907105DMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ901066KMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ56839DMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ44879KMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ60548BMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ60783BMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ65039CMedline Industries, Inc. · Cardiovascular procedure kit1 recall1 report
- Medline Industries, Inc. DYNJ80609DMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. CDS983723JMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ0161262CMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ81581BMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ37284KMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ85109Medline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ85118Medline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ85110Medline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ85121Medline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ906175BMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ85637Medline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ908820AMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ900293KMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ66033BMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
- Medline Industries, Inc. DYNJ84017BMedline Industries, Inc. · Cardiovascular procedure kit1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 97846).
- Z-0511-2026 · Open, ClassifiedMEDLINE convenience kits labeled as LOCAL BASIC, REF DYNJ34418M
- Z-0512-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: CATH LAB PACEMAKER PACK, REF DYNJ59818A
- Z-0514-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) CENTRAL LINE PACK, REF DYNJ00281P; 2) FREE FLAP PACK, REF DYNJ68213C.
- Z-0515-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) BREAST BIOPSY PACK-LF, REF DYNJ0160598C; 2) BIOPSY BREAST PACK, REF DYNJ65361A; 3) BREAST BIOPSY/MASTECTOMY, REF DYNJ908839A.
- Z-0516-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) HEAD AND NECK, REF CDS984259O; 2) HEAD AND NECK, REF CDS984259P; 3) MINOR ENT HARPER PACK-LF, REF DYNJ0160700F; 4) MAJOR ENT HARPER PAC…
- Z-0517-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MAJOR LAPAROTOMY CDS, REF CDS860015W; 2) MAJOR LAPAROTOMY CDS, REF CDS860015X; 3) MINOR LAPAROTOMY CDS, REF CDS860016R; 4) MINOR LAPARO…
- Z-0518-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: PORT INSERTION PACK, REF DYNJ81597
- Z-0519-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) ACH PLASTICS BREAST-LF, REF CDS983639K; 2) BREAST ABD, REF CDS984267J; 3) PLASTIC PACK, REF DYNJ00264M; 4) BREAST ABDOMINOPLASTY MZ PK-…
- Z-0520-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MINOR SINGLE BASIN PACK, REF DYNJ37698L; 2) BASIN PACK, REF DYNJ50123D; 3) MAJOR BASIN PACK, REF DYNJ59816A; 4) OSC BASIN PACK, REF DYN…
- Z-0521-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) GENERAL LAPAROSCOPY, REF CDS930027W; 2) GENERAL MAJOR CDS, REF CDS980245X; 3) BASIC GENERAL CDS, REF CDS980566F; 4) TOTAL KNEE CDS, REF…
- Z-0522-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) BASIC NEURO PACK, REF CDS780202R; 2) ACDF CDS, REF CDS941061M; 3) NEURO PACK-LF, REF DYNJ0038440C; 4) NEURO VP SHUNT/VAGAL NERVE-RF, RE…
- Z-0523-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MAJOR VAGINAL HARPER PACK-LF, REF DYNJ0161768G; 2) ACH MAJOR VAGINAL PACK, REF DYNJ67757B.
- Z-0524-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY CDS #34-RF, REF CDS920099S; 2) GYN LAPAROSCOPY CDS-LF, REF CDS983764J; 3) ROBOTIC, REF CDS984262N; 4) ROBOTIC, REF CDS9…
- Z-0525-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: CIRCUMCISION PACK, REF DYNJ16826O
- Z-0526-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) C-SECTION OR 30 CDS, REF CDS820075W; 2) C-SECTION, REF CDS984261J; 3) C-SECTION CDS, REF CDS985282F; 4) C-SECTION PACK, REF DYNJ02577D;…
- Z-0527-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) GYN LAPAROTOMY HARPER PACK-LF, REF DYNJ0160684F; 2) MAJOR LITHOTOMY PACK-LF, REF DYNJ0425778O; 3) MINOR VAGINAL #76-RF, REF DYNJ27434R; …
- Z-0528-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: GP-LEEP PACK-LF, REF PHS396969004F
- Z-0529-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MINOR EYE TRAY #81, REF DYNJ27466S; 2) MINOR EYE TRAY #81, REF DYNJ27466T.
- Z-0530-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, REF CDS780119V; 2) BASIC BACK CDS, REF CDS780147N; 3) INSTRUMENTED BACK CDS, REF CDS780148R; 4) NEURO-LAMI…
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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