PCC, Rebecca's Natural Food
Reason Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the antibiotic, Chloramphenicol.
Free Form Amino Acids L-Arginine 7 L-Ornithine Complex With Alpha-Lipoic Acid recall
Recalled by Nexgen Pharma, Inc. · Colorado Springs, CO, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Nexgen Pharma is recalling a certain lot of dietary supplement L-Arginine L-Ornithine Alpha Lipoic Acid Capsules due to subpotency of the Alpha Lipoic Acid ingredient.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Free Form Amino Acids L-Arginine 7 L-Ornithine Complex With Alpha-Lipoic Acid, Promotes Circulation and Muscle Development, Dietary Supplement, 50 Vegetarian Capsules, Gluten Free, Serving Size 2 Capsules. Each product is produced for a specific customer with their distribution information on the label. A general label template was provided with attachment B information. Product is sold in 50 and 100 ct bottles.
Quantity: 4571 bottles.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot number 412567.
Where it was sold
Nationwide.
FDA's distribution note: Distributed to large and small retailers located nationwide as well as two foreign locations (Canada and Netherlands).
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Nexgen Pharma, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 15, 2013
- In FDA report of
- May 1, 2013
- Terminated
- Sep 6, 2013
- FDA recall number
- F-1338-2013 · event 64907
- Official record
- FDA enforcement report search