Reported Aug 14, 2024 · Ongoing

Medline procedure kits labeled as

MEDLINE INDUSTRIES, LP - Northfield

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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

12 of 12 products

Products covered by this recall
#Product as published
1CONTINUOUS BLOCK, Pack Number DYNJRA0960C
2COMBINED SPINAL AND EPIDURAL, Pack Number DYNJRA1268C
3WAL- UNIVERSAL BLOCK TRAY, Pack Number DYNJRA1638C
4BASIC DIAGNOSTIC TRAY, Pack Number DYNJRA1928
5PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040
6UNIVERSAL BLOCK TRAY, Pack Number DYNJRA2097
7PAIN TRAY, Pack Number DYNJRA2230
8CONTINUOUS EPIDURAL, Pack Number PAIN1766A
9CONTINUOUS/CSE TRAY, Pack Number PAIN1856
10CONTINUOUS/CSE TRAY, Pack Number PAIN1856A
1120G SINGLE DOSE EPIDURAL, Pack Number PAIN2047
1220G SINGLE DOSE EPIDURAL/CHLOR, Pack Number PAIN2048
Lot codes and dates

48 of 48 products

Products covered by this recall
#Product as published
1DYNJRA0960C , Lot Number 23CBH823
2DYNJRA0960C , Lot Number 23EBC905
3DYNJRA0960C , Lot Number 23EBV028
4DYNJRA0960C , Lot Number 23HBO071
5DYNJRA0960C , Lot Number 24BBI322
6DYNJRA1268C , Lot Number 22GLB081
7DYNJRA1268C , Lot Number 22HLA566
8DYNJRA1268C , Lot Number 22ILA092
9DYNJRA1268C , Lot Number 22LLA800
10DYNJRA1268C , Lot Number 23DLA368
11DYNJRA1268C , Lot Number 23FLA942
12DYNJRA1268C , Lot Number 23GLA321
13DYNJRA1268C , Lot Number 23HLA910
14DYNJRA1268C , Lot Number 23ILA593
15DYNJRA1638C , Lot Number 23EBA854
16DYNJRA1638C , Lot Number 23GBE493
17DYNJRA1638C , Lot Number 23KBJ159
18DYNJRA1928 , Lot Number 22EBD354
19DYNJRA1928 , Lot Number 22JBO947
20DYNJRA1928 , Lot Number 23CBO440
Amount recalled
1,679,067 units in total

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

Stop using this product now

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.

Using this product could cause serious injury, illness or death — stop using it now.

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, 6:24 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.