KVK-Tech, Inc. recalls Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10…
- Recall date
- May 5, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1057-2016
- FDA classification
- Class III
- Brand / firm
- KVK-Tech, Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Discoloration: presence of scuffing marks on tablets.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
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