FDA Drug recall D-0680-2017
Donepezil HCl tablets, 10mg, packaged in 10x10 blister packs per carton (100 Unit Dose) container, Rx only, Manufactured by Sandoz, Inc., 5…
- FDA Drug
- Class III
- terminated
- Published 2017-05-03
On 2017-05-03 the FDA classified a Class III recall of Donepezil HCl tablets, 10mg, packaged in 10x10 blister packs per carton (100 Unit Dose) container, Rx only, Manufactured by Sandoz, Inc., 5… by Mckesson Packaging Services, citing supotent: Out of Specification result for assay test during routine stability testing.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0680-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-01-04 |
| Published | 2017-05-03 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Mckesson Packaging Services |
| Distribution | CO, LA, OH |
Product
Donepezil HCl tablets, 10mg, packaged in 10x10 blister packs per carton (100 Unit Dose) container, Rx only, Manufactured by Sandoz, Inc., 506 Carnegie Center, Suite 400, Princeton, NJ 08805, Distributed by: McKesson Packaging Services, 7101 Weddington Rd, Concord, NC 28027, NDC 63739-678-10
Reason
Supotent: Out of Specification result for assay test during routine stability testing.
Identifiers
| code_info | Lot #0111593, Exp. 05/2017 |
|---|
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-0680-2017%22
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