FDA Food recall F-0757-2014
8532 Kirkman MaxEnzComp w/DP packaged in unlabeled 120-capsule bottles (SKU 53854)
- FDA Food
- Class II
- terminated
- Published 2013-12-25
On 2013-12-25 the FDA classified a Class II recall of 8532 Kirkman MaxEnzComp w/DP packaged in unlabeled 120-capsule bottles (SKU 53854) by National Enzyme, citing firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0757-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-30 |
| Published | 2013-12-25 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | National Enzyme |
| Distribution | US |
Product
8532 Kirkman MaxEnzComp w/DP packaged in unlabeled 120-capsule bottles (SKU 53854)
Reason
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Identifiers
| code_info | Lot #'s: 53854008, 53854010, 53854012, 53854013, and 53854014 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0757-2014%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.