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Faria Limited LLC dba Sheffield Pharmaceuticals

Faria Limited LLC dba Sheffield Pharmaceuticals Recalls

All product recalls associated with Faria Limited LLC dba Sheffield Pharmaceuticals.

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Recall Summary

Total Recalls

1000

Past Year

593

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 8401–8420 of 10391 recalls

Triple Antibiotic Ointment (Sheffield Pharmaceuticals) – Stability Failure (2013)

Failed Stability Specifications: Unable to meet shelf life expiry.

Class IIILow

FDAMay 28, 2013CA, GA, PA +1 more• Faria Limited LLC dba Sheffield Pharmaceuticals

Eyebright Topical Eye Rinse (Wise Woman Herbals) – Sterility Concern (2013)

Lack of Assurance of Sterility; Lack of Assurance of Sterility; product not manufactured under sterile conditions as required for ophthalmic drug products

Class IIModerate

FDAMay 27, 2013Nationwide• Earthlabs, Inc. DBA Wise Woman Herbals

Veggie Burger (Mother Earth) – Salmonella risk (2013)

Salmonella

The product was manufactured with a Soy Protein Isolate manufactured by CHS, Inc and may be contaminated with Salmonella.

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Class IIModerate

FDAMay 23, 2013Nationwide• Mother Earth International LLC

1% Low Fat Cottage Cheese (HP Hood) – metal fragments (2013)

Possible presence of metal fragments.

Class IIModerate

FDAMay 22, 2013AL, AZ, CA +17 more• HP Hood LLC

4% Cottage Cheese (HP Hood) – metal fragments (2013)

Possible presence of metal fragments.

Class IIModerate

FDAMay 22, 2013AL, AZ, CA +17 more• HP Hood LLC

Cottage Cheese with Chive (HP Hood) – metal fragments (2013)

Possible presence of metal fragments.

Class IIModerate

FDAMay 22, 2013AL, AZ, CA +17 more• HP Hood LLC

Lidocaine Hydrochloride Dextrose Injection (Baxter) – sterility port leakage (2013)

Lack of Assurance of Sterilty: Specific lot numbers of these products have been identified for potential administration port leakage. The potential for leakage is the result of a manufacturing issue which occurred during the sealing of the closure assembly at the administration port.

Class IIModerate

FDAMay 21, 2013Nationwide• Baxter Healthcare Corp.

5% Dextrose Injection (Baxter) – sterility port leakage (2013)

Lack of Assurance of Sterility: Specific lot numbers of these products have been identified for potential administration port leakage. The potential for leakage is the result of a manufacturing issue which occurred during the sealing of the closure assembly at the administration port.

Class IIModerate

FDAMay 21, 2013Nationwide• Baxter Healthcare Corp.

Sodium Chloride Injection (Baxter) – sterility port leakage (2013)

Class IIModerate

FDAMay 21, 2013Nationwide• Baxter Healthcare Corp.

Zolpidem Tartrate Tablets (American Health) – mispackaging risk (2013)

Unit Dose Mispackaging: This recall event is due to a random undetected packaging issue which could increase the potential for a small number of individual unit dose blisters to be packed with more than one tablet.

Class IIModerate

FDAMay 21, 2013Nationwide• American Health Packaging

This recall involves two models of Optimus Infrared Quartz Radiant heaters with model numbers H-5210, produced in 2011 and H-5211, produced in 2012. The model number and the year of production appear on a label on the back of the heater. The recalled heaters are white and are approximately 12-inches wide by 13-inches tall by 6-inches deep. "Optimus" is printed on the top left of the heater. The control knob is located on the top right side of the heater.

CPSCMay 15, 2013Nationwide• Dongguang Hong-Hwa Electric Co. Ltd.