Z-0104-2018 Class II Terminated

Recalled by Terumo BCT, Inc. — Lakewood, CO

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