8532 Kirkman MaxEnzComp w/DP recall
8532 Kirkman MaxEnzComp w/DP packaged in unlabeled 120-capsule bottles (SKU 53854)
Why was 8532 Kirkman MaxEnzComp w/DP recalled?
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #'s: 53854008, 53854010, 53854012, 53854013, and 53854014
- Product
- 8532 Kirkman MaxEnzComp w/DP packaged in unlabeled 120-capsule bottles (SKU 53854)
- Recalling firm
- National Enzyme Co
- Quantity
- 3642 bottles.
- Distribution
- Domestic distribution of the product is nationwide with direct accounts in 27 states in all geographical regions. Foreign distribution consists of direct accounts in the following countries: Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.
- Recall date
- December 25, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (food)