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Purely American, Inc.

Purely American, Inc. Recalls

All product recalls associated with Purely American, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 20721–20740 of 25002 recalls

Long Island Seafood Chowder Mix (Purely American) – Unlisted Wheat (2013)

The firm was notified by the Ohio Department of Agriculture that several of their labels are missing the the allergin declaration contains wheat.

Class IIModerate

FDAMar 12, 2013CT, DE, FL +17 more• Purely American, Inc.

Aniracetam and Choline Capsules (Palmer Natural) - Unapproved Drugs (2013)

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Class IIModerate

FDAMar 11, 2013CA, FL, ID• Palmer Natural Products

BoostYourGrade Capsules (Palmer) – Unapproved Drug (2013)

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Class II

1...1035 103610371038 1039...1251

Page 1037 of 1251Next

Moderate

FDAMar 11, 2013CA, FL, ID• Palmer Natural Products

Piracetam & Choline Capsules (Palmer Natural) - Unapproved Drugs (2013)

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Class IIModerate

FDAMar 11, 2013CA, FL, ID• Palmer Natural Products

Nootropa Cognitive Supplement (Palmer Natural) - Unapproved Drugs (2013)

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Class IIModerate

FDAMar 11, 2013CA, FL, ID• Palmer Natural Products

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

Oxiracetam & Choline Capsules (Palmer) – Unapproved Drug (2013)

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Class IIModerate

FDAMar 11, 2013CA, FL, ID• Palmer Natural Products

Aniracetam & Choline Capsules (Palmer Natural) - Unapproved Drugs (2013)

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Class IIModerate

FDAMar 11, 2013CA, FL, ID• Palmer Natural Products

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

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.

Brain Defogger Capsules (Palmer) – Unapproved Drug (2013)

Marketed Without an Approved NDA/ANDA: The products are unapproved drugs

Class IIModerate

FDAMar 11, 2013CA, FL, ID• Palmer Natural Products

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.

Class IIILow

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.

Class IIILow

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.

Class IIILow

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.

Class IIILow

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.

Class IIILow

FDAMar 7, 2013Nationwide• Novartis Consumer Health

Venlafaxine Tablets (Zydus) - Broken Tablet Defect (2013)

Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive amount of broken and/or chipped tablets in the bottle.

Class IIModerate

FDAMar 5, 2013Nationwide• Zydus Pharmaceuticals USA Inc

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.