Pain medications can be a sensitive subject—especially when they require close supervision from medical professionals. However, this recall presents a different concern than usual, one that may affect both human and veterinary care.
Sun Pharmaceutical Industries, Inc. has initiated a nationwide recall of 13,728 bottles of gabapentin, a medication commonly used for nerve pain, restless leg syndrome, and partial seizures. The recall affects two varieties of the drug: 12,876 bottles containing 300-milligram dosages and 852 bottles containing 400-milligram dosages.
Gabapentin, as explained by the Cleveland Clinic, is often prescribed to manage pain caused by conditions like shingles, while PetMD notes its use in veterinary settings for animals dealing with pain, seizures, or anxiety.
The reason for the recall is cited as cross-contamination, though specifics remain unclear. It is not yet known whether individual tablets are contaminated or if another drug might have inadvertently made its way into the packaging. If your gabapentin bottles match the following details, it’s recommended to consult a doctor or pharmacist for guidance on a replacement:
Affected 300-milligram (mg) bottles:
Quantity: 500 or 1,000 capsules
National Drug Codes (NDC): 62756-138-05, 62756-138-04
Lot Numbers:
HAD1458A, Exp. Date: 04/2025
HAD2718A, Exp. Date: 07/2025
HAD3432A, Exp. Date: 08/2025
Affected 400-milligram (mg) bottles:
Quantity: 500 or 1,000 capsules
National Drug Codes (NDC): 62756-139-05, 62756-139-04
Lot Numbers:
HAD1712B, Exp. Date: 03/2025
HAD1712C, Exp. Date: 03/2025
The FDA has classified the recall as a Class III risk, meaning that while the recalled product is unlikely to cause health problems, it fails to meet FDA regulations for labeling or manufacturing.
If you believe your medication may be affected by this recall, it is important to check the details on your prescription and discuss any concerns with a healthcare professional as soon as possible.
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