Reported Apr 2, 2025 · Ongoing

Medline 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?

Medline procedure kits labeled as

6 of 6 products

Products covered by this recall
#Product as published
1L S GYN PACK, Pack Number DYNJ65616C
2MAIN CYSTO, Pack Number DYNJ61371A
3OB PACK-LF, Pack Number DYNJ20720C
4PELVISCOPY PACK-LF, Pack Number DYNJ0415776N
5POSTERIOR EYE PACK-LF, Pack Number PHS656483I
6ROBOTICS PACK-LF, Pack Number DYNJ0046667A
Lot codes and dates

6 of 6 products

Products covered by this recall
#BarcodesProduct as published
11019348979680340193489796804Lot Number 23LMF217A; 2) Pack Number DYNJ61371A: UDI/DI 10193489796803 (each) 40193489796804 (case)
21088438962056440884389620565Lot Number 21FMA140A; 3) Pack Number DYNJ20720C: UDI/DI 10884389620564 (each) 40884389620565 (case)
31019348941398440193489413985Lot Number 21EMF438A; 4) Pack Number DYNJ0415776N: UDI/DI 10193489413984 (each) 40193489413985 (case)
41088994280676840889942806769Lot Number 22CMD073A; 5) Pack Number PHS656483I: UDI/DI 10889942806768 (each) 40889942806769 (case)
51088994216039640889942160397Lot Number 23GMB728A; 6) Pack Number DYNJ0046667A: UDI/DI 10889942160396 (each) 40889942160397 (case)
6Lot Number 22CMD979A
Amount recalled
570 units

This recall covers 29 products

The agency filed one notice per product. You are reading one of them; the other 28 are below.

16 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

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, 5:41 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.