FDA Drug recall D-1111-2022
Sumatriptan Succinate Tablets, 100 mg, 9 (1 x 9) Unit-of- use tablets box, Rx only, MFG: Sun Pharmaceuticals, NDC 62756-522-69
- FDA Drug
- Class II
- terminated
- Published 2022-06-15
On 2022-06-15 the FDA classified a Class II recall of Sumatriptan Succinate Tablets, 100 mg, 9 (1 x 9) Unit-of- use tablets box, Rx only, MFG: Sun Pharmaceuticals, NDC 62756-522-69 by Mckesson Medical Surgical Corporate Office, citing cGMP deviations: Temperature abuse.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1111-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-04-13 |
| Published | 2022-06-15 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Mckesson Medical Surgical Corporate Office |
| Distribution | US |
Product
Sumatriptan Succinate Tablets, 100 mg, 9 (1 x 9) Unit-of- use tablets box, Rx only, MFG: Sun Pharmaceuticals, NDC 62756-522-69
Reason
cGMP deviations: Temperature abuse
Identifiers
| ndc | 62756-520-83 |
|---|---|
| ndc | 62756-520-88 |
| ndc | 62756-520-08 |
| ndc | 62756-520-18 |
| ndc | 62756-520-69 |
| ndc | 62756-520-93 |
| ndc | 62756-520-01 |
| ndc | 62756-521-83 |
| ndc | 62756-521-88 |
| ndc | 62756-521-08 |
| ndc | 62756-521-18 |
| ndc | 62756-521-69 |
| ndc | 62756-521-93 |
| ndc | 62756-521-01 |
| ndc | 62756-522-83 |
| ndc | 62756-522-88 |
| ndc | 62756-522-08 |
| ndc | 62756-522-18 |
| ndc | 62756-522-69 |
| ndc | 62756-522-93 |
| ndc | 62756-522-01 |
| code_info | McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee fo…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. |
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-1111-2022%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.