HARVEST — Class II medical device recall Z-0103-2018
Terminated recall by Terumo BCT, Inc., reported 2017-11-22, distributed in CA, MO, NY, PA, TX, VA, WI. The patient labels included in the BMAC system procedure packs, catalog numbers 51416 and 51423, are printed w
| Recall number | Z-0103-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Terumo BCT, Inc., Lakewood, CO, United States |
| Recall initiated | 2017-10-20 |
| Classified | 2017-11-16 |
| Reported by FDA | 2017-11-22 |
| Terminated | 2020-08-21 |
| Distributed | CA, MO, NY, PA, TX, VA, WI |
| Countries outside the US | AT, ES, TR |
| Quantity | 30 units |
| Reason classes | labeling, sterility |
| Lot numbers | 04A9938 |
| Model numbers | 51416 |
Product
HARVEST(R) TERUMOBCT, BMAC-30-07 Bone Marrow Procedure Pack, Private Practice / Clinical Use Only, REF 51416, 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0103-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.