Teva Pharmaceuticals USA Recall: Buprenorphine Transdermal System 5 mcg/hour, 4 transderma
Teva Pharmaceuticals USA Recall: Buprenorphine Transdermal System 5 mcg/hour, 4 transderma is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Teva Pharmaceuticals USA; Product: Buprenorphine Transdermal System 5 mcg/hour, 4 transdermal systems/4 disposal units per carton, Rx Only, Manufac
| Recalling firm | Teva Pharmaceuticals USA |
|---|---|
| Product | Buprenorphine Transdermal System 5 mcg/hour, 4 transdermal systems/4 disposal units per carton, Rx Only, Manufactured by: 3M Drug Delivery Systems, 19901 Nordhoff street, Northridge, CA 91324 USA, Manufactured for: Teva Pharmaceuticals USA Inc., North Wales, PA 19454, carton NDC: 0093-3656-40, patch NDC: 0093-3656-21. |
| Reason for recall | Failed Stability Specifications: Below specification result for buprenorphine release rate. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide in the U.S. and PR |
| Recall initiated | 20200904 |
| Recall number | D-0003-2021 |
| Category | drug |
| State | NJ |
| Country | United States |
$29/mo
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