FDASeptember 20, 2018device
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
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
What to do
FDA enforcement status: Terminated
Brands named
micro tech nanjingmicromicro tech
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCJunpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Federal Statute for Child-Resistant Packaging of Coin Batteries; Sold on Amazon by JSNJ_Tech Store2026-07-02
- CPSCArizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by 7111495 Canada2026-06-18
- FDARover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV712026-03-27
- CPSCWagner Spray Tech Recalls 900 Series Power Steamers Due to Burn Hazard2026-03-19
- CPSCEvajoy Above-Ground Pools 48 Inches and Taller Recalled Due to Drowning Hazard; Manufactured by Shenzhen Danya Tech2026-02-26
- CPSCJohnson Health Tech Expands Recall to Include Matrix Retail and Vision Treadmills Due to Fire Hazard2026-01-22
- CPSCArizer Solo II Portable Vaporizers Recalled Due to Fire and Burn Hazards; Imported by 7111495 Canada2025-09-18
- CPSCFieldsheer Apparel Technologies Recalls Heated Socks Due to Injury Hazard2025-08-07
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