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Home > Recalled Products > Pet Care Products > Lack of Sterility > Norbrook Laboratories Limited Subcutaneous injectable drug products

Recall: Norbrook Laboratories Limited Subcutaneous injectable drug products

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On 2019-04-29, the FDA announced that Norbrook Laboratories Limited is conducting a recall on Subcutaneous injectable drug products due to a possible . The recalled products were sold under the brand name(s) Norbrook Laboratories Limited during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 1 pet care products recalls due to potential lack of sterility, including irrigating solutions and corneal repair drops, fluid therapies for pets and more.

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Norbrook Laboratories Limited, Logo
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Company Contact Information:

Name: Norbrook Laboratories Limited
Phone: 866-591-5777

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Detailed Recall Information



Regions Where Sold: Nationwide

Product Description: Veterinary Products

Brand Name(s): Norbrook Laboratories Limited

Reason for Recall: Lack of Sterility

Official Recall Date: 2019-04-29


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Additional information provided by the FDA.gov:

Norbrook Laboratories Limited of Newry, Northern Ireland is expanding the recall of subcutaneous injectable drug products that began in early March 2019. Norbrook is adding to the recall four lots of Enroflox 100 Injection (enrofloxacin), two lots of Noromectin Injection (ivermectin) and one lot of Ivermax 1% Injection (ivermectin) to the veterinarian/consumer level as a precautionary measure as product sterility cannot be assured. There is a concern that if the sterility of these products has been compromised, use of these products could result in introduction of infectious agents to the animal. This may result in the need for medical intervention(s) including, but not limited to the need for supportive care, antibiotics, and/or antifungal drugs. Read More.


More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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