Drug product
Recothrom Thrombin Topical (Recombinant), 5,000 units, packaged in a box containing a 5000-unit vial of RECOTHROM with a 5-mL prefilled diluent syringe (containing sterile 0.9% sodium chloride, USP), a sterile needle-free transfer device, a 5-mL sterile empty syringe, and a pre-printed label, Rx only, MFG: Baxter, NDC# 0338-0322-01
D-1082-2022
Product summary
- Event
- Event 89646
- Status
- Terminated
- Classification
- Class II
- Quantity
- 110 cartons/5000 units each
- Official record key
drug-enforcement:D-1082-2022
Official wording
Reason: cGMP deviations: Temperature abuse
Code information: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Distribution pattern: USA nationwide.
Derived failure modes
-
Manufacturing or process control
cGMP deviations