Drug recall: Various Eye drops recalled due to this reason

This drug recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

251
Drug product Recall
Drug Recall

Drug recall

The firm issued a press release on 15/11/2023 regarding the drug recall. This press release amendment includes corrected NDC numbers for the mentioned products.

Summary

  • Company Announcement Date:January 19, 2024
  • FDA Publish Date: January 22, 2024
  • Product Type: Drugs
  • Reason for Announcement: Device & Drug Safety Potential Safety Concerns
  • Company Name: Kilitch Healthcare India Limited
  • Brand Name: Multiple brands
  • Product Description: Lubricant Eye Drops & Multi-Symptom Eye Drops

Company Announcement

Mumbai, Maharashtra, Kilitch Healthcare India Limited is issuing an amendment in the last Nationwide press release dated November 13, 2023 issued for nationwide recall of various eye drops.

There are corrections in product NDC No for the below mentioned products.

ProductProduct InformationNDC NO
(wrongly
Mention is last
press release)
NDC Nos
(Corrected, to
be read as)
Retailer /
Label
LUBRICANT GEL DROPS 15 MLCarboxymethylcellulose Sodium Eye Drops 1.0% W/V11822-9706-511822-4540-5Rite Aid
LUBRICANT EYE DROPS 15ML (TWIN PACK)Carboxymethylcellulose Sodium Eye Drops 0.5% W/V11822-9707-511822-4811-5Rite Aid

Related news: Drug recall: These Eye drops Recalled – A Closer Look at Unsafe Practices


These products were distributed nationwide to wholesalers, retailers, and via the product distributor, Velocity Pharma LLC.

Kilitch Healthcare India Limited, is notifying its distributor Velocity Pharma LLC and its distributor Velocity Pharma LLC shall be further notifying the wholesalers and retailers via mail of this voluntary recall and is arranging for return of all impacted products listed above.

Consumers, distributors and retailers that have any product which is being recalled should cease distribution of the product.

Consumers should stop using the recalled eye drops and may return any of the above listed products to the place of purchase.

This drug recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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