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Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical Recalls

All product recalls associated with Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical.

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Recall Summary

Total Recalls

1000

Past Year

197

Class I (Serious)

410

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 2001–2020 of 3552 recalls

Testosterone Cypionate Progesterone (Fusion IV) – CGMP deviation (2017)

CGMP Deviations

Class IIModerate

FDAJul 12, 2017CA, IN• Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Progesterone Injection (Apothecary By Design) – Container Issue (2017)

Lack of Processing Controls: The metal container closure adheres to the rubber stopper on some of the units of the batch which can impact the integrity of the container closure.

Class IIModerate

FDAJun 5, 2017Nationwide• Apothecary By Design

NutriHeal Cholesterol Supplement (Herbmed) – undeclared milk (2017)

Undeclared Milk

Product contains undeclared milk.

1...99 100101102 103...178

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Class I

High

FDAMay 26, 2017Nationwide• Herbmed USA Company Inc.

Kiteboard Control Systems (Cabrinha) – Injury Risk (2017)

Fire/Burn Risk

The component subject to recall is the stainless steel POWER BRACKET SEAT (PBS) and the lower front line that connects with the landing line on the Overdrive 1X Recoil with Fireball or Quickloop, Overdrive 1X Trimlite with Fireball or Quickloop, 1X Trimlite with Fireball or Quickloop and the Chaos 1X Control system models. The stainless steel PBS is mounted on the top of the depower mainline between one of the lower front lines and the landing line. The PBS is used as a stopping point for one of the flying lines while allowing the activation of the 1X security landing line. Model numbers included in the recall are: KS7CSODFR, KS7CSODQR, KS7CSODFC, KS7CSODQC, KS7CSFXFC, KS7CSFXQC and KS7CSCHFX. Only models with "2017 1X" printed on a cloth tab attached to the bungee line restrainers at the end of the bars are included in this recall.

CPSCMay 17, 2017Nationwide• Cabrinha Kites, a subsidiary of Pryde Group Americas, of Doral, Fla.

Denali Moose Tracks Cheesecake (Father's Table) – labeling error (2017)

Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.

Class IIILow

FDAMay 9, 2017FL, GA, IN• The Father's Table, LLC

Hydrocortisone Lotion (Qualitest) – Superpotent Drug (2017)

Superpotent Drug: above specification for the assay.

Class IIILow

FDAMay 8, 2017Nationwide• Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Chicken & Waffle Sandwich (Fourth Street BBQ) – listeria risk (2017)

Listeria

Product has the potential to be contaminated with Listeria monocytogenes.

Class IIModerate

FDAMay 8, 2017Nationwide• Fourth Street Barbeque, Inc.

Protein Bar (Herbalife) – undeclared fish gelatin (2017)

Herbalife is recalling Protein Bar-Peanut Butter because it may contain a trace amount of fish gelatin.

Class IIILow

FDAMay 1, 2017Nationwide• Herbalife International Of America Inc

HEB Texas Toast – Rubber Contamination (2017)

Presence of rubber in the product.

Class IIModerate

FDAApr 20, 2017TX• HEB Retail Support Center

HEB White Bread – Rubber Contamination (2017)

Presence of rubber in the product.

Class IIModerate

FDAApr 20, 2017TX• HEB Retail Support Center

Hill Country Fare Wheat Sandwich (HEB) – Rubber Contamination (2017)

Presence of rubber in the product.

Class IIModerate

FDAApr 20, 2017TX• HEB Retail Support Center

Hill Country Fare Thin Sandwich (HEB) – Rubber Contamination (2017)

Presence of rubber in the product.

Class IIModerate

FDAApr 20, 2017TX• HEB Retail Support Center

White Wheat Bread (HEB) – Rubber Contamination (2017)

Presence of rubber in the product.

Class IIModerate

FDAApr 20, 2017TX• HEB Retail Support Center