Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to Single-Use Biopsy Forceps box contains incorrect product, instead...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Micro-Tech (Nanjing) Co., Ltd. directly.
Affected Products
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
Quantity: 1360 pcs
Why Was This Recalled?
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Micro-Tech (Nanjing) Co., Ltd.
Micro-Tech (Nanjing) Co., Ltd. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report