Z-0104-2018 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- November 22, 2017
- Initiation Date
- October 20, 2017
- Termination Date
- August 21, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 281 units
Product Description
HARVEST(R) TERUMOBCT, BMAC2-120-01Bone Marrow Procedure Pack, REF 51423, Rx Only, STERILE EO
Reason for Recall
The patient labels included in the BMAC system procedure packs, catalog numbers 51416 and 51423, are printed with an incorrect lot number, catalog number, and expiry date; the lot number on the procedure pack box label is correct. The expiration noted was not beyond initiation date of the recall. Since the product is noted as sterile, the clearance for K103340, K052925 and K991430 raises question if product was cleared with a sterility claim. Further post-market follow-up will be required to assess the safety risk of the product.
Distribution Pattern
CA, Co, MO, NY, PA, TX, VA, WI, Turkey, Austria, Spain
Code Information
UDI Case: 35020583514233, 51423 Each: 05020583514232, Lot 04A9939