Reported Sep 18, 2024 · Ongoing

Medline 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 Convenience kits labeled as

11 of 11 products

Products covered by this recall
#Product as published
1CVC INSERTION PACK, Pack Number CVI4720A
2CVC INSERTION PACK, Pack Number CVI4720AH
3CATHETER INSERTION KIT CLABSI , Pack Number CVI4880
4CHEST INSERTION PACK-LF , Pack Number DYNJ17634D
5URETEROSCOPY, Pack Number DYNJ45882A
6TONSIL PACK CATH, Pack Number DYNJ65199A
7CATH PLACEMENT RIB FRACTURE , Pack Number DYNJ66475B
8UROLOGY ROBOTIC PACK, Pack Number DYNJ80211C
9UROLOGY ROBOTIC PACK, Pack Number DYNJ80211CH
10UROLOGY PK, Pack Number DYNJ80252C
11PORT INSERTION PACK , Pack Number DYNJ81597
Lot codes and dates

74 of 74 products

Products covered by this recall
#Product as published
1CVI4720A , Lot Number 23DLA715
2CVI4720A , Lot Number 23ELB184
3CVI4720A , Lot Number 23GLA187
4CVI4720A , Lot Number 23ILA599
5CVI4720A , Lot Number 23ILA949
6CVI4720A , Lot Number 23JLA318
7CVI4720A , Lot Number 23JLB102
8CVI4720AH, Lot Number 23DLA715
9CVI4720AH, Lot Number 23ELB184
10CVI4720AH, Lot Number 23GLA187
11CVI4720AH, Lot Number 23ILA599
12CVI4720AH, Lot Number 23ILA949
13CVI4720AH, Lot Number 23JLA318
14CVI4720AH, Lot Number 23JLB102
15CVI4880, Lot Number 22LBM567
16CVI4880, Lot Number 23HBU762
17DYNJ17634D , Lot Number 23LBB611
18DYNJ45882A , Lot Number 21HBE710
19DYNJ45882A , Lot Number 21HBO631
20DYNJ45882A , Lot Number 21JBD536

This recall covers 106 products

The agency filed one notice per product. You are reading one of them; the other 105 are below.

93 more are in the archive.

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, 4:55 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.