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American Licorice Co

American Licorice Co Recalls

All product recalls associated with American Licorice Co.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 16341–16360 of 21320 recalls

Black Licorice Twists (American Licorice) – Elevated Lead (2012)

CA Dept. of Public Health collected random samples of Red Vines Black Licorice and found elevated levels of lead in the product.

Class IIModerate

FDAAug 21, 2012Nationwide• American Licorice Co

Stir Fried Tofu (Pacific NW Tofu) – Incomplete Label (2012)

Laceration Risk

Soy was partially declared on the label because the ingredient list is cut off at the right side of the label.

Class IIModerate

FDAAug 21, 2012IN, OR• Pacific Northwest Tofu, LLC

ProBalance Protein (Protica) – Botulinum contamination risk (2012)

Product not sufficiently acidified (equilibrium pH higher than 4.6), therefore it has the potential to be contaminated with Clostridium botulinum

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Class IIModerate

FDAAug 17, 2012Nationwide• Protica, Inc

ProBalance Protein Shake (Protica) – Botulinum contamination risk (2012)

Product not sufficiently acidified (equilibrium pH higher than 4.6), therefore it has the potential to be contaminated with Clostridium botulinum

Class IIModerate

FDAAug 17, 2012Nationwide• Protica, Inc

Major Oral Peroxide (Axcentria) – Unstable Expiration (2012)

Stability data does not support expiration date: Stability data indicates the Carbamide Peroxide will degrade below acceptable levels within the 24-month expiration date printed on the packaging.

Class IIILow

FDAAug 17, 2012MI• Axcentria Pharmaceuticals LLC

Protein Wave (Protica) – Botulinum contamination risk (2012)

Product not sufficiently acidified (equilibrium pH higher than 4.6), therefore it has the potential to be contaminated with Clostridium botulinum

Class IIModerate

FDAAug 17, 2012Nationwide• Protica, Inc

Protein Shots (Protica) – Botulinum contamination risk (2012)

Product not sufficiently acidified (equilibrium pH higher than 4.6), therefore it has the potential to be contaminated with Clostridium botulinum

Class IIModerate

FDAAug 17, 2012Nationwide• Protica, Inc

Babylicious Cloth Crib Fringe – Strangulation Risk (2012)

The product is a narrow fabric strip connecting several individual fabric triangles. It is designed to be attached to the side rail of a crib or along window valences or curtain rods. The product was sold in a variety of colors and patterns and with two fringes in each package.

CPSCAug 16, 2012Nationwide• Babylicious Products Inc., of Vancouver, British Columbia, Canada

DYNAMIC TIRE SAILUN S825 Tire Recall: TIRES:SIDEWALL

Dynamic Tire Corporation (Dynamic) is recalling certain Sailun S825 commercial application tires, size 385/65R22.5, produced between March and April 2012. The inner-liner thickness may be thinner than specification requirements.

NHTSAAug 16, 2012Nationwide• DYNAMIC TIRE

Baby Seats (Bumbo) – Fall Hazard (2012)

The bottom of the Bumbo seat is round and flat with a diameter of about 15 inches. It is constructed of a single piece of molded foam and comes in various colors. The seat has leg holes and the seat back wraps completely around the child. On the front of the seat in raised lettering is the word "Bumbo" with the image of an elephant on top. The bottom of the seat has the following words: "Manufactured by Bumbo South Africa Material: Polyurethane World Patent No. PCT: ZA/1999/00030." The back of the seat has several warnings and seats manufactured since 2008 have an additional label on the front of the seat warning against use on raised surfaces.

CPSCAug 15, 2012Nationwide• Bumbo International Trust, of South Africa

Prometh VC Plain (Actavis) – Stability Degradation (2012)

Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.

Class IIILow

FDAAug 14, 2012Nationwide• Actavis Mid Atlantic LLC

Choletec Kit (Bracco) – Particulate Matter Risk (2012)

Presence of Particulate Matter; potential for charcoal particulates

Class IIILow

FDAAug 14, 2012Nationwide• Bracco Diagnostic Inc

Prometh VC with Codeine (Actavis) – Stability Degradation (2012)

Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.

Class IIILow

FDAAug 14, 2012Nationwide• Actavis Mid Atlantic LLC

Fresh Mahi Mahi Fillets (Atlantic Fisheries) – High Histamine (2012)

Atlantic Fisheries recalled 580 lbs of Mahi Mahi Fillets due to histamine levels over 50 ppm.

Class IIModerate

FDAAug 13, 2012AL, FL, IN +1 more• Atlantic Fisheries

Nature's Harvest Pine Nuts (American Importing) – Undeclared peanuts (2012)

Undeclared Nuts

Amport Foods is recalling one lot of pine nuts because there may be undeclared Peanuts present in the product.

Class IIModerate

FDAAug 8, 2012AL, AZ, CA +21 more• American Importing Co, Inc

Doxazosin Tablets (Mylan) – Product Cross Contamination (2012)

Cross Contamination w/Other Products: During stability testing chromatographic review revealed extraneous peaks identified as acetaminophen and codeine.

Class IIModerate

FDAAug 7, 2012Nationwide• Mylan Pharmaceuticals Inc.