🔍 RecallPedia

MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C

Class I - Dangerous
🏥 Medical Devices Recalled: October 27, 2025 Medline Industries Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 10193489621532 (each) 40193489621533 (case), Lot Number 25FMJ081
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Medline Industries, LP
Reason for Recall:
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C

Product Codes/Lot Numbers:

UDI/DI 10193489621532 (each) 40193489621533 (case), Lot Number 25FMJ081

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0886-2026

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