Sheep Blood, Defibrinated - Catalog Number 212390, Unit 60 ml.
FDA device recall Z-1321-04 · posted 2004-08-07 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Co.
- Reason for recall
- Sheep Blood products may be contaminated with a Brucella species (B. ovis).
- Action taken
- Distributors were notified by fax, all customers were notified by fax with a UPS overnight delivery of hard copy of recall letter to same customers. BD International was notified be e-mail. Distributor fax indicated that BD required their customer lists immediately due to the nature of the recall event. BD received all Distributor customer lists on the same day (7/2/04). Will monitor the number of consignees non-responding to the recall through sending a letter that contains a form that we ask the end-user to return. Response forms will be reconciled. Distribution of the affected lots ceased on 7/1/04. Customers are asked to discard their inventory.
- Root cause
- Other
- Status
- Terminated
- Product code
- JSO
- Quantity affected
- 7 vials
- Distribution
- 83 (76 end-users, 3 international BD facilities and 4 distributors) worldwide.
- Date initiated
- 2004-07-02
- Date posted
- 2004-08-07
- Date terminated
- 2004-12-21
- Location
- Sparks, MD
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