Medline brand, medical procedure convenience kits, labeled… recallZ-0720-2025 · MEDLINE INDUSTRIES, LP - Northfield · initiated Nov 6, 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
Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods
FDA root cause category: Nonconforming Material/Component
What the company is doing
An IMMEDIATE ACTION REQUIRED MEDICAL DEVICE RECALL notification letter dated 11/7/24 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 on affected 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-24-209-FGX1 Recall Code: Recall 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-0720-2025
- Status
- Open, Classified
- Initiated by the company
- Nov 6, 2024
- Posted by the FDA
- Dec 20, 2024
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 6467 kits
- Product code
- OGR
- Distribution
- US Nationwide. Canada.
Product description
Medline brand, medical procedure convenience kits, labeled as: 1) SINUS CDS-1, SKU CDS982901F; 2) NASAL PACK, SKU DYNJ17493G; 3) FESS PACK-POB, SKU DYNJ33520A; 4) SINUS PACK, SKU DYNJ44845G; 5) SINUS PACK, SKU DYNJ48330B; 6) ENT PACK, SKU DYNJ50572; 7) ENT PACK, SKU DYNJ53573A; 8) ENT HUTCH, SKU DYNJ58856A; 9) PACK NASAL, SKU DYNJ60111A; 10) PACK NASAL, SKU DYNJ60111B; 11) ENT CUSTOM PACK, SKU DYNJ63052C; 12) ENT PACK, SKU DYNJ64256D; 13) FESS/SEPTOPLASTY PACK, SKU DYNJ64509B; 14) SINUS ENDOSCOPY PACK, SKU DYNJ65644; 15) ACOUSTICS SHSC-LF, SKU DYNJ66749; 16) TRANSPHENOIDAL PACK, SKU DYNJ67423A; 17) TRANSPHENOIDAL PACK, SKU DYNJ67423B; 18) ENT PACK, SKU DYNJ68102B; 19) E N T PACK, SKU DYNJ80526B; 20) NASAL PACK, SKU DYNJ81280; 21) ENT FESS PACK, SKU DYNJ81420A; 22) HEAD AND NECK PACK, SKU DYNJ81934; 23) HEAD AND NECK PACK - 51597, SKU DYNJ81934A; 24) HEAD AND NECK ENT PACK, SKU DYNJ83679A; 25) HEAD NECK PACK HC, SKU DYNJ84270; 26) TRANSPHENOIDAL PACK-LF, SKU DYNJ85422; 27) NASAL SEPTAL, SKU DYNJ901299A; 28) NASAL SEPTAL, SKU DYNJ901299B; 29) PACK TRANSPHENOIDAL, SKU DYNJ905685D; 30) SEPTOPLASTY, SKU DYNJ906474C; 31) LEFORTE MANDIBLE, SKU DYNJ906839A; 32) NASAL MHS, SKU DYNJ908545A; 33) NASAL MHS, SKU DYNJ908545B; 34) ENT, SKU DYNJ909128A; 35) ENT, SKU DYNJ909128C; 36) ENT, SKU DYNJ909128D; 37) ENT, SKU DYNJ909128F; 38) SINUS PACK, SKU DYNJ909370
Code information (models, lots, serial numbers)
Show the full code information (4k characters)
UDI-DI: CDS982901F, 10889942216970 (each), 40889942216971 (case), Lot Numbers: 23HBQ152; UDI-DI: DYNJ17493G, 10195327224424 (each), 40195327224425 (case), Lot Numbers: 23GBW775; UDI-DI: DYNJ33520A, 10884389851333 (each), 40884389851334 (case), Lot Numbers: 23HDB834; UDI-DI: DYNJ44845G, 10889942712311 (each), 40889942712312 (case), Lot Numbers: 23HBF195; UDI-DI: DYNJ48330B, 10195327113506 (each), 40195327113507 (case), Lot Numbers: 23HBO622; UDI-DI: DYNJ50572, 10889942008476 (each), 40889942008477 (case), Lot Numbers: 23GBR940; UDI-DI: DYNJ53573A, 10193489201635 (each), 40193489201636 (case), Lot Numbers: 23GBS356; UDI-DI: DYNJ58856A, 10193489750263 (each), 40193489750264 (case), Lot Numbers: 23HBO870; UDI-DI: DYNJ60111A, 10193489246995 (each), 40193489246996 (case), Lot Numbers: 21JMB783 21HMF433 21GMD178 21FMC923 20IMB575; UDI-DI: DYNJ60111B, 10195327527617 (each), 40195327527618 (case), Lot Numbers: 24HMC974 24GMA899 24FMB079 24EMC108 24DMD791 24CMG320; UDI-DI: DYNJ63052C, 10195327101312 (each), 40195327101313 (case), Lot Numbers: 22KME394 22KMA630 22JMD852 22GMG160 22EMG974 22DMF954 22CMC565; UDI-DI: DYNJ64256D, 10195327452773 (each), 40195327452774 (case), Lot Numbers: 23HBA766; UDI-DI: DYNJ64509B, 10195327323745 (each), 40195327323746 (case), Lot Numbers: 23HBC092; UDI-DI: DYNJ65644, 10193489283204 (each), 40193489283205 (case), Lot Numbers: 23HBA753; UDI-DI: DYNJ66749, 10193489375947 (each), 40193489375948 (case), Lot Numbers: 21ABT938 21ABO570 20JBS998 20HBM389; UDI-DI: DYNJ67423A, 10195327163402 (each), 40195327163403 (case), Lot Numbers: 24DLA092 24BLA235 23KLA058 23ILB043 23ILA503 23HLB296 23HLB011 23FLA068 23DLA463 23DLA185 23BLA617 22LLA582 22KLA652 22HLA029 22GLA884; UDI-DI: DYNJ67423B, 10195327686871 (each), 40195327686872 (case), Lot Numbers: 24GLB018 24FLA258 24ELA763 24DLA759; UDI-DI: DYNJ68102B, 10195327699369 (each), 40195327699360 (case), Lot Numbers: 24IBB348 24GBB791 24EBA114; UDI-DI: DYNJ80526B, 10195327211059 (each), 40195327211050 (case), Lot Numbers: 23HBF568; UDI-DI: DYNJ81280, 10195327102968 (each), 40195327102969 (case), Lot Numbers: 22HMF910; UDI-DI: DYNJ81420A, 10195327322601 (each), 40195327322602 (case), Lot Numbers: 24CBL416 23LBK136 23IBR308 23HBD265 23GBJ044 23FBK113 23EBN716 23BBQ143; UDI-DI: DYNJ81934, 10195327156817 (each), 40195327156818 (case), Lot Numbers: 23EBG024 23BBC727 22JBJ632 22HBH399; UDI-DI: DYNJ81934A, 10195327413019 (each), 40195327413010 (case), Lot Numbers: 24DBK564 24DBB486 24CBG998 24BBV700 24ABD320 23HBO084 23GBG012; UDI-DI: DYNJ83679A, 10195327459727 (each), 40195327459728 (case), Lot Numbers: 24HBP441 24GBF665 24BBO428 23LBS373 23JBD663 23IBN314; UDI-DI: DYNJ84270, 10195327349103 (each), 40195327349104 (case), Lot Numbers: 23GBC274; UDI-DI: DYNJ85422, 10195327499716 (each), 40195327499717 (case), Lot Numbers: 24FDA925 24ADB100; UDI-DI: DYNJ901299A, 10889942010349 (each), 40889942010340 (case), Lot Numbers: 21FBC250 20JBO761 20IBH831 20FBM501; UDI-DI: DYNJ901299B, 10193489923384 (each), 40193489923385 (case), Lot Numbers: 22FBU440 22OBC118 22OBC120 22ABA377 21JBJ197 21IBM868 21GBO441; UDI-DI: DYNJ905685D, 10198459024139 (each), 40198459024130 (case), Lot Numbers: 24IDB382; UDI-DI: DYNJ906474C, 10195327221355 (each), 40195327221356 (case), Lot Numbers: 24HDA228 24EDA811 24DDB542 23LDB493 23GDA771 23DDA732 22IDB976; UDI-DI: DYNJ906839A, 10195327092528 (each), 40195327092529 (case), Lot Numbers: 22JMB394; UDI-DI: DYNJ908545A, 10195327384166 (each), 40195327384167 (case), Lot Numbers: 23JBV681; UDI-DI: DYNJ908545B, 10195327593124 (each), 40195327593125 (case), Lot Numbers: 24HBI988 24FBS776 24FBA297 24ABT058; UDI-DI: DYNJ909128A, 10195327326739 (each), 40195327326730 (case), Lot Numbers: 23EBD903 23DBD851; UDI-DI: DYNJ909128C, 10195327458416 (each), 40195327458417 (case), Lot Numbers: 23JBO251 23HBI313; UDI-DI: DYNJ909128D, 10195327516321 (each), 40195327516322 (case), Lot Numbers: 24EBC023 24CBK211 24BBM816 24ABR742 23LBQ695 23LBM416; UDI-DI: DYNJ909128F, 10198459055256 (each), 40198459055257 (case), Lot Numbers: 24HBV054 24GBN495; UDI-DI: DYNJ909370, 10195327319038 (each), 40195327319039 (case), Lot Numbers: 24BMA818 24AMG256 23LMF420 23LMB722 23LMA458 23CME287;
Devices named in this recall
38 devices in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNJ53573AMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ58856AMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ906839AMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ67423AMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ17493GMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ60111BMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ67423BMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ50572Medline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. CDS982901FMedline Industries, Inc. · Ear, nose, and throat surgical tray3 recalls0 reports
- Medline Industries, Inc. DYNJ65644Medline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ66749Medline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ901299BMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ63052CMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ81280Medline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ48330BMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ80526BMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ64509BMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ909128AMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ84270Medline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ64256DMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ909128CMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ83679AMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ85422Medline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ909128DMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ68102BMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ33520AMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ44845GMedline Industries, Inc. · Ear, nose, and throat surgical tray2 recalls0 reports
- Medline Industries, Inc. DYNJ60111AMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ81934Medline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ906474CMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ909370Medline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ81420AMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ908545AMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ81934AMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ908545BMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ905685DMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ909128FMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ901299AMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 95806).
- Z-0717-2025 · Open, ClassifiedMAJOR NEURO PACK-LF Convenience kit, SKU DYNJ0578916X. Convenience kits used for various procedures.
- Z-0718-2025 · Open, ClassifiedFESS-MB PACK-LF Convenience kit, SKU DYNJ0888159I. Convenience kits used for various procedures..
- Z-0719-2025 · Open, ClassifiedDIEP FLAP Convenience kit, SKU DYNJ910120. Convenience kits used for various procedures.
- Z-0721-2025 · Open, ClassifiedMedline brand, medical procedure convenience kits, labeled as: 1) MVFF/FIBU #54-RF , SKU DYNJ21927R; 2) DIEP FLAP, SKU DYNJ910120A
- Z-0722-2025 · Open, ClassifiedSEPTOPLASTY PACK Convenient kit, SKU DYNJ44759F. Convenience kits used for various procedures.
- Z-0723-2025 · Open, ClassifiedMedline brand, medical procedure convenience kits, labeled as: 1) CRANIOTOMY, SKU CDS982719X; 2) MVFF/FIBU #54-RF, SKU DYNJ21927Q; 3) MVFF/FIBU #54-RF, SKU DYNJ21927S; 3) NEURO PED…
- Z-0724-2025 · Open, ClassifiedMedline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119T; 2) NEURO KIT, SKU CDS981327Q; 3) NEURO POSTERIOR SPINE PACK-LF, SKU…
- Z-0725-2025 · Open, ClassifiedKIT,SPINE LH Convenience kit, SKU DYNJ906448A.
- Z-0726-2025 · Open, ClassifiedMedline brand, medical procedure convenience kits, labeled as: 1) LAMINECTOMY CDS-LF, SKU CDS780045N; 2) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119U; 3) NEURO CRANIOTOMY CDS #36…
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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