Rx CHOICE brand LIQUID VITAMIN C
Reason The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.
FERROUS SULFATE ELIXIR 220 mg/ recall
Recalled by Hi-Tech Pharmacal Co., Inc. · Amityville, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY 11701
Quantity: 581 units
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 62110, exp. date 04/2015
Where it was sold
Louisiana New Jersey Ohio Puerto Rico Texas
FDA's distribution note: NJ, OH, TX, LA, and Puerto Rico
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Hi-Tech Pharmacal Co., Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 23, 2014
- In FDA report of
- Mar 11, 2015
- Terminated
- May 8, 2017
- FDA recall number
- F-1380-2015 · event 70097
- Official record
- FDA enforcement report search
Other recalls by Hi-Tech Pharmacal Co., Inc.
Rx CHOICE brand LIQUID VITAMIN C
Reason Out-of-specification results for pH.