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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Medline Medical Convenience Kits Recalled for Syringe Leaks and Breakage

Agency Publication Date: March 18, 2025
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Summary

Medline Industries, LP is recalling 1,336 medical convenience kits, including C-Section and Eye Pack procedure kits, because they contain plastic syringes that may leak or break. These syringes were part of a March 2024 FDA Safety Alert due to identified quality issues. No incidents or injuries have been reported at this time.

Risk

Defective syringes can leak or break during medical procedures, which may lead to errors in medication delivery, delays in treatment, or potential injury to patients.

What You Should Do

  1. This recall affects Medline procedure kits labeled as C SECTION (Pack Number DYNJ909098) and EYE PACK (Pack Number VAL038BSCLC).
  2. Identify if your kits are affected by checking for lot numbers 23GBK039Z or 40193489244442 and verifying the catalog/pack numbers printed on the kit packaging.
  3. Stop using the recalled kits immediately.
  4. Contact Medline Industries or your medical distributor to arrange for the return, replacement, or correction of the affected kits.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding this safety alert.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction/replacement

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Medline C SECTION Procedure Kit
Model / REF:
DYNJ909098
Lot Numbers:
23GBK039Z
GTIN:
10195327273132
40195327273133

Pack Number DYNJ909098; Recall #: Z-1393-2025

Product: Medline EYE PACK Procedure Kit
Model / REF:
VAL038BSCLC
Lot Numbers:
40193489244442
GTIN:
10193489244441
40195327273133

Pack Number VAL038BSCLC; Recall #: Z-1394-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96372
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Sold By: Hospital supply chains; Medical distributors
Manufactured In: United States
Units Affected: 2 products (456 kits; 880 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.