Every recall we track for KENIL HEALTHCARE PRIVATE LIMITED — 20 in all — plus the complaints and injury reports the public filed about them.
Kenil Healthcare is recalling Curahongos 1% Clotrimazole topical lotion due to CGMP deviations. The product may not meet safety standards. Consumers should check the lot number on the label.
Kenil Healthcare recalls Cinnafresh anticavity gel toothpaste with sodium fluoride 0.22% due to CGMP deviations. Affected lots expire May 2026 through September 2026. No remedy specified in recall notice.
Kenil Healthcare recalls Kofal Athletes Penetrating Pain Relief Ointment due to CGMP deviations. This external analgesic may not meet quality standards. Consumers should check product details and contact the manufacturer for instructions.
Kenil Healthcare is recalling Rapidol Triple Antibiotic First Aid Ointment due to CGMP deviations. This may affect product safety. Check the NDC 55758-440-02 label for affected items.
Kofal Original Penetrating Pain Relieving Ointment (methyl salicylate 12%) with CGMP deviations is being recalled. This recall affects 4 oz jars distributed by Pharmadel LLC. Consumers should check NDC 55758-106-04 for affected products.
Kenil Healthcare is recalling Curahongos antifungal cream (Clotrimazole 1%) due to CGMP deviations. This may affect safety. Check product details to see if you have the recalled item.
Kenil Healthcare recalls Nature Mint toothpaste due to manufacturing deviations. This product may have quality issues from improper production processes.
Kenil Healthcare recalls Nature Mint toothpaste with CGMP deviations. Affected lots expire 05/31/2026 to 09/30/2026. Consumers should check labels for NDC 53247-131-02 and lots B0015-B0110.
Kenil Healthcare recalls Maximum Security Anticavity Gel Toothpaste with CGMP deviations. Affected lots expire May 2026 through September 2026. No remedy specified in official notice.
Kenil Healthcare recalls specific lots of Maximum Security Anticavity Gel Toothpaste (Sodium Fluoride 0.22%) due to CGMP deviations. Consumers should check product details and contact the company for instructions.
Kenil Healthcare is recalling Nature Mint Anticavity Fluoride Toothpaste due to CGMP deviations. This affects specific lots and expiration dates. Consumers should check their product details and contact the manufacturer for instructions.
Kenil Healthcare is recalling 17% salicylic acid bottles (NDC 55758-423-15) made in India with CGMP deviations. Consumers should contact Pharmadel LLC for details.
Kenil Healthcare recalls Rapidol Maximum Strength Hydrocortisone 1% Anti-Itch Cream due to CGMP deviations. Consumers should check product details and contact the manufacturer for instructions.
Kenil Healthcare recalls Artridon Glucosamine topical analgesic for arthritis pain due to manufacturing quality control deviations. This product may not meet safety standards.
Kenil Healthcare recalls Optim V Anti-Itch Cream due to manufacturing deviations. This cream contains Benzocaine 20% and Resorcinol 3% and may pose quality risks. Consumers should check product details and contact the manufacturer for guidance.
Kenil Healthcare recalls Maximum Security Anticavity Gel Toothpaste with CGMP deviations. Products made in India, distributed by Bob Barker Co. Inc. in NC. Affected lots expire May 2026 through August 2026.
Kenil Healthcare recalls Maximum Security Anticavity Gel Toothpaste with sodium fluoride 0.22% due to CGMP deviations. Products may not meet safety standards. Consumers should check product details and contact the company for action.
Kenil Healthcare recalls Nature Mint toothpaste with CGMP deviations. Products made in India, distributed by Bob Barker Co. Inc. in NC. Consumers should check NDC codes and expiration dates for affected lots.
Kenil Healthcare recalls Nature Mint Anticavity Fluoride Toothpaste due to CGMP deviations. This may affect safety standards. Check product details to see if you have the recalled batch.
Kenil Healthcare recalls Nature Mint Anticavity Fluoride Toothpaste with CGMP deviations. Products made in India, distributed by Bob Barker Co. Inc. in NC. Check NDC 53247-131-03 and lot numbers for affected items.
