Braintree HalfLytely and Bisacodyl Tablet Bowel Prep Kit — Class III drug recall D-911-2013
Terminated recall by Braintree Laboratories Inc., reported 2013-08-28. Defective Container; Small micro fracture observed in the 2-Liter bottle at the fill line resulting in a small
| Recall number | D-911-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Braintree Laboratories Inc., Holbrook, MA, United States |
| Recall initiated | 2013-07-15 |
| Classified | 2013-08-20 |
| Reported by FDA | 2013-08-28 |
| Terminated | 2014-01-21 |
| Quantity | 10,362 kits |
| Reason classes | packaging, device malfunction |
| NDC | 52268-0523-02 |
| Lot numbers | 08/14, 3013002 |
Product
Braintree HalfLytely and Bisacodyl Tablet Bowel Prep Kit (Rx) NDC 52268-523-02
Reason for recall
Defective Container; Small micro fracture observed in the 2-Liter bottle at the fill line resulting in a small leak when patient reconstitutes the bulk powder
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-911-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.