FDA Device recall Z-1382-2021
SUNSTAR Butler Clear Dip, 16 FL OZ, SKU #716PA
- FDA Device
- Class II
- terminated
- Published 2021-04-21
On 2021-04-21 the FDA classified a Class II recall of SUNSTAR Butler Clear Dip, 16 FL OZ, SKU #716PA by Sunstar Americas, citing product may be contaminated with Burkholderia contaminans.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1382-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-03-23 |
| Published | 2021-04-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Sunstar Americas |
| Distribution | n/a |
Product
SUNSTAR Butler Clear Dip, 16 FL OZ, SKU #716PA
Reason
Product may be contaminated with Burkholderia contaminans.
Identifiers
| code_info | Lot Numbers; 532952, 535180, 536513, 536514, 539487, 551038, 551039 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1382-2021%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.