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Medline Convenience kits labeled as recallZ-3033-2024 · MEDLINE INDUSTRIES, LP - Northfield · initiated Apr 8, 2024

Class II Open, Classified All recalls posted in September 2024

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

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.

FDA root cause category: Under Investigation by firm

What the company is doing

Medline Industries LP issued a recall notice to its consignees on 04/08/2024 via letter delivered via USPS and email. The notice explained the issue, provided a link to for information pertaining to the risk involved https://www.fda.gov/medical-devices/safety-communications/update-evaluating-plastic-syringes-made-china-potential-device-failures-fda-safety-communication) and request these syringes within the convenience be discarded, except for circumstances where no alternative syringes are readily available. If these syringes must be used, closely monitor for leaks, breakage, and any other problems, and report any quality issues to Medline and the FDA. Distributors were directed to notify their customers. The firm issued a second recall notice (an expansion) on 05/02/2024 using the same methods.

Recall details

Recall number
Z-3033-2024
Recall class
Class II
Status
Open, Classified
Initiated by the company
Apr 8, 2024
Posted by the FDA
Sep 6, 2024
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product code
FMF
FDA submissions
K103830
Distribution
Worldwide distribution.

Product description

Medline Convenience kits labeled as: 1) SYRINGE CNTRL 10ML RED L/L LP , Pack Number DYNJSYCPP10R ; 2) SYRINGE CNTRL 10ML YEL L/L LP , Pack Number DYNJSYCPP10Y ; 3) SYRINGE KIT , Pack Number NAM0004; 4) SYR 10ML L/S, Pack Number OEM11623 ; 5) JAPAN 3ML SYRINGE , Pack Number SAMPCJ006; 6) JAPAN 5ML SYRINGE, Pack Number SAMPCJ007; 7) JAPAN 10ML SYRINGE, Pack Number SAMPCJ008; 8) JAPAN 20ML SYRINGE, Pack Number SAMPCJ009; 9) JAPAN 30ML SYRINGE, Pack Number SAMPCJ010; 10) JAPAN 60ML SYRINGE, Pack Number SAMPCJ011

Code information (models, lots, serial numbers)

Show the full code information (1k characters)

DYNJSYCPP10R , Lot Number 22JBR164 ; DYNJSYCPP10Y , Lot Number 22JBR165 ; NAM0004, Lot Number 21DDB223 ; NAM0004, Lot Number 21HDC569 ; NAM0004, Lot Number 21IDB793 ; NAM0004, Lot Number 21JDA347 ; NAM0004, Lot Number 21LDA148 ; OEM11623 , Lot Number 21GBQ995 ; OEM11623 , Lot Number 22BBC557 ; OEM11623 , Lot Number 22CBH284 ; OEM11623 , Lot Number 19BBF348 ; OEM11623 , Lot Number 19DBI184 ; OEM11623 , Lot Number 22EBE833 ; OEM11623 , Lot Number 19QBB707 ; OEM11623 , Lot Number 19FBK375 ; OEM11623 , Lot Number 19GBY960 ; OEM11623 , Lot Number 19HBH787 ; OEM11623 , Lot Number 19HBO770 ; OEM11623 , Lot Number 23ABH043 ; OEM11623 , Lot Number 19KBX346 ; OEM11623 , Lot Number 19LBK179 ; OEM11623 , Lot Number 20BBC515 ; OEM11623 , Lot Number 20BBS501 ; OEM11623 , Lot Number 20CBB499 ; OEM11623 , Lot Number 20CBB674 ; OEM11623 , Lot Number 20FBA919 ; OEM11623 , Lot Number 20HBT942 ; OEM11623 , Lot Number 20LBK683 ; OEM11623 , Lot Number 20XBD345 ; OEM11623 , Lot Number 21FBG914 ; SAMPCJ006, Lot Number 24ADC130 ; SAMPCJ007, Lot Number 24ADC129; SAMPCJ008, Lot Number 24ADC128 ; SAMPCJ009, Lot Number 24ADC127 ; SAMPCJ010, Lot Number 24ADC126 ; SAMPCJ011, Lot Number 24ADC125

Other devices under the same FDA submission

2 devices cleared under K103830 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 94583).

Sources and updates

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