Every recall we track for LUPIN SOMERSET — 13 in all, from 2018–2019 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls on record by year — 13 drug.
Lupin Somerset recalls 60mg Morphine Sulfate Extended-Release Tablets due to failed impurities and degradation specifications. Rx-only bottles with specific NDC and lot numbers affected.
Lupin Somerset recalls Gavilyte-N oral solutions with incorrect lemon flavor labeling. The product lists "natural lemon flavor" but should be orange or cherry. No immediate action needed as it's a labeling error.
Lupin Somerset recalls fluocinolone acetonide topical solution 0.01% 60mL bottles due to impurities from oxidative degradation. This may cause serious injury. Stop using and contact for return.
Lupin Somerset recalls specific lots of Nitrofurantoin Oral Suspension due to subpotent drug levels. This may not provide effective treatment for urinary tract infections. Consumers should check lot numbers and contact the manufacturer for details.
Lupin Somerset recalls Fluocinolone Acetonide Topical Solution 0.01% 60ml bottles due to impurities detected during stability testing. Affected lots may pose safety risks.
13 recalls from LUPIN SOMERSET are on record with U.S. safety agencies, from 2018–2019.
LUPIN SOMERSET recalls Morphine Sulfate Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured by: Novel Laboratories, Inc., dated Apr 10, 2019. Every LUPIN SOMERSET recall is listed on this page, newest first.
The most common reasons on record: Failed Impurities/Degradation Specifications (5).
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
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