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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Bausch & Lomb Ophthalmic Solution Recalled for Temperature Abuse

Agency Publication Date: September 20, 2024
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Summary

McKesson Medical-Surgical Inc. has recalled 27 bottles of Bausch & Lomb Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile). The eye drops were exposed to improper temperatures above the required drug label specifications during distribution to two medical facilities in Maryland and Virginia. Using medication that has been stored at incorrect temperatures can compromise the safety and effectiveness of the drug.

Risk

Exposure to temperatures above specified limits can lead to the chemical degradation of the medication. This may result in decreased potency, making the numbing solution ineffective during medical procedures, or potentially causing irritation to the patient's eyes.

What You Should Do

  1. This recall affects 15 mL bottles of Bausch & Lomb Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile) with NDC 24208-730-06.
  2. Identify affected products by checking for lot numbers 476261, 479751, or 479741 with an expiration date of 3/31/2026.
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (15 mL)by Bausch & Lomb
Variants: Sterile, Rx only, 0.5%
Lot Numbers:
476261 (Exp 3/31/2026)
479751 (Exp 3/31/2026)
479741 (Exp 3/31/2026)
NDC:
24208-730-06

Recall #: D-0661-2024; Product was distributed to two medical facilities in MD and VA.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95333
Status: Resolved
Manufacturer: Mckesson Medical-Surgical Inc. Corporate Office
Sold By: Medical facilities
Manufactured In: United States
Units Affected: 27 bottles
Distributed To: Maryland, Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.