Reported Jan 1, 2025 · Ongoing
Medline brand, medical procedure convenience kits, labeled as
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline brand, medical procedure convenience kits, labeled as
38 of 38 products
| Model / number | Product as published |
|---|---|
CDS982901F | SINUS CDS-1 |
DYNJ17493G | NASAL PACK |
DYNJ33520A | FESS PACK-POB |
DYNJ44845G | SINUS PACK |
DYNJ48330B | SINUS PACK |
DYNJ50572 | ENT PACK |
DYNJ53573A | ENT PACK |
DYNJ58856A | ENT HUTCH |
DYNJ60111A | PACK NASAL |
DYNJ60111B | PACK NASAL |
DYNJ63052C | ENT CUSTOM PACK |
DYNJ64256D | ENT PACK |
DYNJ64509B | FESS/SEPTOPLASTY PACK |
DYNJ65644 | SINUS ENDOSCOPY PACK |
DYNJ66749 | ACOUSTICS SHSC-LF |
DYNJ67423A | TRANSPHENOIDAL PACK |
DYNJ67423B | TRANSPHENOIDAL PACK |
DYNJ68102B | ENT PACK |
DYNJ80526B | E N T PACK |
DYNJ81280 | NASAL PACK |
- Lot codes and dates
38 of 38 products
Products covered by this recall # Barcodes Product as published 1 1088994221697040889942216971CDS982901F, 10889942216970 (each), 40889942216971 (case), Lot Numbers: 23HBQ152 2 1019532722442440195327224425UDI-DI: DYNJ17493G, 10195327224424 (each), 40195327224425 (case), Lot Numbers: 23GBW775 3 1088438985133340884389851334UDI-DI: DYNJ33520A, 10884389851333 (each), 40884389851334 (case), Lot Numbers: 23HDB834 4 1088994271231140889942712312UDI-DI: DYNJ44845G, 10889942712311 (each), 40889942712312 (case), Lot Numbers: 23HBF195 5 1019532711350640195327113507UDI-DI: DYNJ48330B, 10195327113506 (each), 40195327113507 (case), Lot Numbers: 23HBO622 6 1088994200847640889942008477UDI-DI: DYNJ50572, 10889942008476 (each), 40889942008477 (case), Lot Numbers: 23GBR940 7 1019348920163540193489201636UDI-DI: DYNJ53573A, 10193489201635 (each), 40193489201636 (case), Lot Numbers: 23GBS356 8 1019348975026340193489750264UDI-DI: DYNJ58856A, 10193489750263 (each), 40193489750264 (case), Lot Numbers: 23HBO870 9 1019348924699540193489246996UDI-DI: DYNJ60111A, 10193489246995 (each), 40193489246996 (case), Lot Numbers: 21JMB783 21HMF433 21GMD178 21FMC923 20IMB575 10 1019532752761740195327527618UDI-DI: DYNJ60111B, 10195327527617 (each), 40195327527618 (case), Lot Numbers: 24HMC974 24GMA899 24FMB079 24EMC108 24DMD791 24CMG320 11 1019532710131240195327101313UDI-DI: DYNJ63052C, 10195327101312 (each), 40195327101313 (case), Lot Numbers: 22KME394 22KMA630 22JMD852 22GMG160 22EMG974 22DMF954 22CMC565 12 1019532745277340195327452774UDI-DI: DYNJ64256D, 10195327452773 (each), 40195327452774 (case), Lot Numbers: 23HBA766 13 1019532732374540195327323746UDI-DI: DYNJ64509B, 10195327323745 (each), 40195327323746 (case), Lot Numbers: 23HBC092 14 1019348928320440193489283205UDI-DI: DYNJ65644, 10193489283204 (each), 40193489283205 (case), Lot Numbers: 23HBA753 15 1019348937594740193489375948UDI-DI: DYNJ66749, 10193489375947 (each), 40193489375948 (case), Lot Numbers: 21ABT938 21ABO570 20JBS998 20HBM389 16 1019532716340240195327163403UDI-DI: DYNJ67423A, 10195327163402 (each), 40195327163403 (case), Lot Numbers: 24DLA092 24BLA235 23KLA058 23ILB043 23ILA503 23HLB296 23HLB011 23FLA068 23DLA463 23DLA185 23BLA617 22LLA582 22KLA652 22HLA029 22GLA884 17 1019532768687140195327686872UDI-DI: DYNJ67423B, 10195327686871 (each), 40195327686872 (case), Lot Numbers: 24GLB018 24FLA258 24ELA763 24DLA759 18 1019532769936940195327699360UDI-DI: DYNJ68102B, 10195327699369 (each), 40195327699360 (case), Lot Numbers: 24IBB348 24GBB791 24EBA114 19 1019532721105940195327211050UDI-DI: DYNJ80526B, 10195327211059 (each), 40195327211050 (case), Lot Numbers: 23HBF568 20 1019532710296840195327102969UDI-DI: DYNJ81280, 10195327102968 (each), 40195327102969 (case), Lot Numbers: 22HMF910 - Amount recalled
- 6467 kits
This recall covers 17 products
The agency filed one notice per product. You are reading one of them; the other 16 are below.
4 more are in the archive.
Where it was sold
- Nationwide
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
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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