🔍 RecallPedia

MEDLINE Sterile* Needle Counter, 100Ct. Double Magnet / Foam Block, reorder: DYNJNC100F Product Usage: A needle counter is intended to be used safely and easily accounting for used, disposable surgical sharps during a surgical procedure. The product does not come in contact with the surgical site or the patient.

Class I - Dangerous
🏥 Medical Devices Recalled: April 24, 2018 Medline Industries Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: 67016114502, 67017014501, 67017024503, 67017034501, 67017044504, 67017054501, 67017054504, 67017064503, 67017074501, 67017074502, 67017084502, 67017094501, 67017104501, 67017114501
  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 Inc
Reason for Recall:
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle Counters.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

MEDLINE Sterile* Needle Counter, 100Ct. Double Magnet / Foam Block, reorder: DYNJNC100F Product Usage: A needle counter is intended to be used safely and easily accounting for used, disposable surgical sharps during a surgical procedure. The product does not come in contact with the surgical site or the patient.

Product Codes/Lot Numbers:

Lot Numbers: 67016114502, 67017014501, 67017024503, 67017034501, 67017044504, 67017054501, 67017054504, 67017064503, 67017074501, 67017074502, 67017084502, 67017094501, 67017104501, 67017114501

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1931-2018

Related Recalls