FDA Drug recall D-1455-2016
Albuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by Contract Pharmaceuticals Limited, Canada, Manufactur…
- FDA Drug
- Class II
- terminated
- Published 2016-08-17
On 2016-08-17 the FDA classified a Class II recall of Albuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by Contract Pharmaceuticals Limited, Canada, Manufactur… by Teva North America, citing presence of Foreign Substance; presence of black particles describes generically as cellulose-based bundles of brown fibrous material.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1455-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-22 |
| Published | 2016-08-17 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Teva North America |
| Distribution | US |
Product
Albuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by Contract Pharmaceuticals Limited, Canada, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA --- NDC 0093-0661-16
Reason
Presence of Foreign Substance; presence of black particles describes generically as cellulose-based bundles of brown fibrous material.
Identifiers
| code_info | Lot # 95113, exp 01/2017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1455-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.