Reported Jan 8, 2025 · Ongoing

Medline custom medical procedure 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?

379 of 379 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS780089V1019348958741840193489587419In sequential order by REF Numbers as listed in product description: , UDI/DI 10193489587418 (EA) 40193489587419 (CS), Lot number 19BLA484
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19DBN638
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19EBN450
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19FBN031
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19JBE273
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19JBI710
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19KBR616
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20BBQ409
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20CBP611
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20EBG877
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20EBS145
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20FBB178
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20FBR886
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20JBH667
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21BBJ070
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21DBH746
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21HBJ414
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21IBA053
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21JBD207
CDS780102K1088994271450640889942714507UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21KBC783
Amount recalled
474300 units

This recall covers 18 products

The agency filed one notice per product. You are reading one of them; the other 17 are below.

5 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.