Recall Z-0237-2019— Micro-Tech (Nanjing) Co., Ltd.
Class II · Terminated
Class II FDA medical device recall by Micro-Tech (Nanjing) Co., Ltd., initiated 2018-09-20, terminated 2019-10-21. FDA's recall record names no specific 510(k) clearance for this event. Product: 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. Reason: Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units.
- Recalling firm
- Micro-Tech (Nanjing) Co., Ltd.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-09-20
- Terminated
- 2019-10-21
- Firm location
- Nanjing, N/A, China
Product 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
Reason for recall
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Data sourced from openFDA. This site is unofficial and independent of the FDA.