Anderson Compounding Pharmacy, Inc. DBA Anderson C Recall: Heparin 20,000 U/Lidocaine 2% 1
Anderson Compounding Pharmacy, Inc. DBA Anderson C Recall: Heparin 20,000 U/Lidocaine 2% 1 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy; Product: Heparin 20,000 U/Lidocaine 2% 10 mL/Sodium Bicarbonate 8.4% 10 mL/S
| Recalling firm | Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy |
|---|---|
| Product | Heparin 20,000 U/Lidocaine 2% 10 mL/Sodium Bicarbonate 8.4% 10 mL/Sterile Water 5 mL, 27 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN. |
| Reason for recall | Lack of sterility assurance. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20190402 |
| Recall number | D-1156-2019 |
| Category | drug |
| State | TN |
| Country | United States |
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