Reported Sep 4, 2024 · Ongoing

Centurion procedure packs, containing Caina syringes, 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?

Centurion procedure packs, containing Caina syringes, labeled as

9 of 9 products

Products covered by this recall
#Product as published
1BREAST BIOPSY KIT, Pack Number DYNDH1512A
2CIRCUMCISION KIT, Pack Number CIT6535
3CIRCUMCISION KIT, Pack Number CIT7095
4CIRCUMCISION TRAY, Pack Number CIT6860A
5CIRCUMCISION TRAY, Pack Number DYNDA2271
6CIRCUMCISION TRAY, Pack Number CIT6720
7CIRCUMCISION TRAY, Pack Number CIT7020
8MEDICAL CIRCUMCISION TRAY, Pack Number CIT6780
9NICU CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6920
Lot codes and dates

41 of 41 products

Products covered by this recall
#Product as published
1DYNDH1512A, Lot Number 2023030190
2CIT6535, Lot Number 2023090580
3CIT7095, Lot Number 2020121190
4CIT7095, Lot Number 2022031590
5CIT6860A, Lot Number 2021111580
6CIT6860A, Lot Number 2022010480
7CIT6860A, Lot Number 2022041880
8CIT6860A, Lot Number 2022053080
9CIT6860A, Lot Number 2022062080
10CIT6860A, Lot Number 2022121280
11CIT6860A, Lot Number 2023032080
12CIT6860A, Lot Number 2023062680
13CIT6860A, Lot Number 2023071780
14CIT6860A, Lot Number 2023090580
15CIT6860A, Lot Number 2023091180
16CIT6860A, Lot Number 2023111380
17CIT6860A, Lot Number 2024020580
18DYNDA2271, Lot Number 2021072890
19CIT6720, Lot Number 2021080390
20DYNDA2271, Lot Number 2021083190

This recall covers 55 products

The agency filed one notice per product. You are reading one of them; the other 54 are below.

42 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, 7:35 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.