B911 Kirkman Max Spectrum E recall
B911 Kirkman Max Spectrum E, packaged unlabeled, 90-capsule bottles (SKU 54255);
Why was B911 Kirkman Max Spectrum E 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 #: 54255000
- Product
- B911 Kirkman Max Spectrum E, packaged unlabeled, 90-capsule bottles (SKU 54255);
- Recalling firm
- National Enzyme Co
- Quantity
- 1138 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)