Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals

Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals Recalls

All product recalls associated with Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

581

Class I (Serious)

91

Most Recent

Dec 2025

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 8281–8300 of 10937 recalls

Well at Wallgreens Antacid (Tarmac/Axara) – Microbial Contamination (2013)

Microbial Contamination of Non-Sterile Products: Lot in question had an elevated microbial count outside of specifications and E. Coli contamination.

Class IIModerate

FDAMar 16, 2013Nationwide• Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals

Avastin (Clinical Specialties) – Sterility Concern (2013)

Lack of Assurance of Sterility; product linked to adverse event reports of endophthalimitis eye infections and FDA inspection findings resulted in concerns regarding quality control processes

Class IIModerate

FDAMar 11, 2013FL, GA, IN +2 more• Clinical Specialties Compounding Pharmacy

Acetic Acid Otic Solution (Hi-Tech Pharmacal) - Subpotent Drug (2013)

1...413 414415416 417...547

Page 415 of 547Next

Subpotent Drug: The product/lot is out-of-specification (OOS) for the assay of acetic acid at the 18-month test station.

Class IIILow

FDAMar 11, 2013Nationwide• Hi-Tech Pharmacal Co., Inc.

4 Way Fast Acting Nasal Spray (Novartis) - Illegible Lot Number (2013)

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

FDAMar 7, 2013Nationwide• Novartis Consumer Health

Myoflex Pain Relieving Cream (Novartis) - Illegible Lot Number (2013)

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

FDAMar 7, 2013Nationwide• Novartis Consumer Health

Nupercainal Ointment (Novartis) - Illegible Lot Number (2013)

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

FDAMar 7, 2013Nationwide• Novartis Consumer Health

4 Way Saline Moisturizing Mist (Novartis) - Illegible Lot Number (2013)

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

FDAMar 7, 2013Nationwide• Novartis Consumer Health

4 Way Nasal Decongestant Spray (Novartis) - Illegible Lot Number (2013)

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

FDAMar 7, 2013Nationwide• Novartis Consumer Health

Snow Blower (Briggs & Stratton) – fire hazard (2013)

The recalled snow blower is 24 inches wide and comes in orange with black. Recalled products have the model number 920014 and serial numbers ranging from 100,000 through 119,039 that can be found on an Ariens-brand label on the lower back panel of the product with the warranty code. There is also a Briggs and Stratton engine model number 13D1370110 F1 labeled on the side of the engine with the serial number range from 12053000000 through 12071699999. Engines with a circular black marker dot located on the right side of the engine base, below the electric starter and just above the oil drain plug, have already been inspected and are not part of this recall.

CPSCMar 5, 2013Nationwide• Briggs & Stratton Corporation, of Milwaukee, Wis.

Ezekiel 4:9 Cinnamon Raisin Cereal (Food For Life) – undeclared almond (2013)

Undeclared Allergen

The firm is recalling Ezekiel 4:9 Sprouted Grain Cereal because the product may be mislabeled and may contain an undeclared allergen - almond.

Class IIModerate

FDAMar 1, 2013Nationwide• Food For Life Baking Company Inc.

Ezekiel 4:9 Golden Flax Cereal (Food For Life) – undeclared almond (2013)

Undeclared Allergen

The firm is recalling Ezekiel 4:9 Sprouted Grain Cereal because the product may be mislabeled and may contain an undeclared allergen - almond.

Class IIModerate

FDAMar 1, 2013Nationwide• Food For Life Baking Company Inc.

Ezekiel 4:9 Original Cereal (Food For Life) – undeclared almond (2013)

Undeclared Allergen

The firm is recalling Ezekiel 4:9 Sprouted Grain Cereal because the product may be mislabeled and may contain an undeclared allergen - almond.

Class IIModerate

FDAMar 1, 2013Nationwide• Food For Life Baking Company Inc.

Fenofibric Acid Tablets (Mutual Pharmaceutical) – Incorrect Labeling (2013)

Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed HDL-C level is detected, fibrate therapy should be withdrawn, and the HDL-C level monitored until it has returned to baseline, and fibrate therapy should not be re-initiated." The labeling for the recalled lots

FDAFeb 27, 2013Nationwide• Mutual Pharmaceutical Company, Inc.

Fenofibric Acid Tablets (Mutual Pharmaceutical) – Incorrect Labeling (2013)

Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed HDL-C level is detected, fibrate therapy should be withdrawn, and the HDL-C level monitored until it has returned to baseline, and fibrate therapy should not be re-initiated." The labeling for the recalled lots

FDAFeb 27, 2013Nationwide• Mutual Pharmaceutical Company, Inc.

FIBRICOR Tablets (Mutual Pharmaceutical) – Incorrect Labeling (2013)

Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed HDL-C level is detected, fibrate therapy should be withdrawn, and the HDL-C level monitored until it has returned to baseline, and fibrate therapy should not be re-initiated." The labeling for the recalled lots

FDAFeb 27, 2013Nationwide• Mutual Pharmaceutical Company, Inc.

Vanilla Almond Granola (Amport Foods) – Undeclared Allergens (2013)

American Importing Co., d/b/a Amport Foods is voluntarily recalling a limited number of packages of its Amport Foods 16 oz Vanilla Almond Granola because they may contain pliable metal wire mesh fragments from a defective flour sifter from a 3rd party vendor.

Class IIModerate

FDAFeb 25, 2013IL, IN, IA +9 more• American Importing Co, Inc

Fruit & Granola Trail Mix (Amport Foods) – Undeclared Allergens (2013)

American Importing Co., d/b/a Amport Foods is voluntarily recalling a limited number of packages of its Amport Foods 16 oz Vanilla Almond Granola because they may contain pliable metal wire mesh fragments from a defective flour sifter from a 3rd party vendor.

Class IIModerate

FDAFeb 25, 2013IL, IN, IA +9 more• American Importing Co, Inc

Orchard Reserve Fiber Blend (Amport Foods) – Undeclared Allergens (2013)

American Importing Co., d/b/a Amport Foods is voluntarily recalling a limited number of packages of its Amport Foods 16 oz Vanilla Almond Granola because they may contain pliable metal wire mesh fragments from a defective flour sifter from a 3rd party vendor.

Class IIModerate

FDAFeb 25, 2013IL, IN, IA +9 more• American Importing Co, Inc

Unbleached All-Purpose Flour (King Arthur) – Foreign Material (2013)

Foreign material

Class IIModerate

FDAFeb 22, 2013Nationwide• The King Arthur Flour Company, Inc.

Unbleached Bread Flour (King Arthur) – Foreign Material (2013)

Foreign material

Class IIModerate

FDAFeb 22, 2013Nationwide• The King Arthur Flour Company, Inc.