FDA Drug recall D-1135-2023
heparin added to 0.9% sodium chloride, 2500 units/500mL (5 units/mL), IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South…
- FDA Drug
- Class II
- terminated
- Published 2023-09-06
On 2023-09-06 the FDA classified a Class II recall of heparin added to 0.9% sodium chloride, 2500 units/500mL (5 units/mL), IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South… by Central Admixture Pharmacy Services, citing lack of Assurance of Sterility:Lack of validation data for sanitization cycles.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1135-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2023-08-17 |
| Published | 2023-09-06 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Central Admixture Pharmacy Services |
| Distribution | US |
Product
heparin added to 0.9% sodium chloride, 2500 units/500mL (5 units/mL), IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-8100-1
Reason
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Identifiers
| code_info | Lot# 36-260045, 36-260046, Exp 9/13/2023. ; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1135-2023%22
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