Every recall we track for Hetero Labs, Ltd. - Unit III — 5 in all, from 2017–2018 — plus the complaints and injury reports the public filed about them.
Recalls on record by year — 5 drug.
Hetero Labs recalls 145mg fenofibrate tablets (Rx only) due to foreign valacyclovir tablets in some bottles. Consumers should check NDC 31722-596-90 and lot E181370.
Hetero Labs recalls 50mg indomethacin capsules that may be deformed, clumped, or melted. These prescription capsules were manufactured for Camber Pharmaceuticals and sold in the US. Consumers should check product details and contact the manufacturer for a remedy.
Hetero Labs recalls 10mg Aripiprazole tablets with CGMP deviations. These tablets may not meet specifications. Stop using if you have the affected lot numbers.
Hetero Labs recalls 40mg Simvastatin tablets due to metallic razor blade found in one bottle. This could cause injury if taken. Consumers should contact the manufacturer for details.
Hetero Labs recalls Levetiracetam Oral Solution (100 mg/mL) due to a foreign screw in the bottle. This could cause injury if the bottle breaks. Contact the manufacturer for details.
5 recalls from Hetero Labs, Ltd. - Unit III are on record with U.S. safety agencies, from 2017–2018.
Hetero Labs, Ltd. - Unit III recalls Fenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway,, dated Sep 12, 2018. Every Hetero Labs, Ltd. - Unit III recall is listed on this page, newest first.
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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