Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40182 (Carton box level) - BF40183(Over shipper level), STERILE

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number - M180409031 Date of Manufacture - 20180409 Use By - 20220408
  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:
Micro-Tech (Nanjing) Co., Ltd.
Reason for Recall:
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40182 (Carton box level) - BF40183(Over shipper level), STERILE

Product Codes/Lot Numbers:

Lot Number - M180409031 Date of Manufacture - 20180409 Use By - 20220408

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0237-2019

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