Z-0237-2019 Class II Terminated
FDA device recall Z-0237-2019 was initiated by Micro-Tech (Nanjing) Co., Ltd. on September 20, 2018 and is designated Class II. Reason for recall: Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units The recall status is terminated (terminated October 21, 2019). Affected quantity: 1360 pcs.
Recall Details
- Product Type
- Devices
- Report Date
- October 31, 2018
- Initiation Date
- September 20, 2018
- Termination Date
- October 21, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1360 pcs
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
Distribution Pattern
US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C.
Code Information
Lot Number - M180409031 Date of Manufacture - 20180409 Use By - 20220408