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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)

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 16121–16140 of 21320 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.

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

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.

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Class IIModerate

FDAMar 5, 2013Nationwide• Zydus Pharmaceuticals USA Inc

Add a Scoop Probiotic (Juice Bar Solutions) – GMO claim (2013)

It was discovered that label for Add a Scoop Probiotic stated that it was GMO free, however manufacturers paperwork did not support the claim.

Class IIILow

FDAMar 4, 2013AZ, CA, FL +7 more• Juice Bar Solutions

Chunk Light Tuna in Oil (Chicken of the Sea) – undeclared ingredient (2013)

Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken of the Sea brand 5-ounce cans of chunk white albacore tuna in water and Chicken of the Sea brand 5-ounce cans chunk light tuna in oil, because the seams on the lids of the cans do not meet the standard for seam quality.

Class IIModerate

FDAMar 4, 2013Nationwide• Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Chunk White Albacore Tuna (Chicken of the Sea) – undeclared ingredient (2013)

Class IIModerate

FDAMar 4, 2013Nationwide• Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Voltaren Gel (Physicians Total Care) - Illegible Lot Number (2013)

Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is being initiated because the lot number and expiration date on the tube may not be legible.

Class IIILow

FDAMar 2, 2013Nationwide• Physicians Total Care, Inc.

Propolis Powder (Beehive Botanicals) – chemical contamination (2013)

Beehive Botanical, Inc is recalling several lots of Propolis 55-60% due to positive identification of Fluvalinate.

Class IIModerate

FDAMar 1, 2013CA, NY• Beehive Botanicals, Inc.

Propolis Chunks (Beehive Botanicals) – chemical contamination (2013)

Beehive Botanical, Inc is recalling several lots of Propolis 55-60% due to positive identification of Fluvalinate.

Class IIModerate

FDAMar 1, 2013CA, NY• Beehive Botanicals, Inc.

Pre-lit Christmas Trees (Balsam Hill) – burn and shock hazard (2013)

Fire/Burn Risk

The artificial Christmas trees are pre-lit with both multi-color and clear lights that are operated by a remote control. Some larger trees have two remote control receiver boxes attached to the tree. The Christmas trees are green and stand between 7 ½ and 15 feet tall. Trees with the following model numbers are included in this recall. The model number is located on the tree's packaging. Date code H1203 is printed on a white label on the back of the remote control box attached to the tree. Model Number Tree Name Lighting Type 6528502 103913 0112 12' Vermont White Spruce™ Color+Clear 6528502 130645 0112 15' California Baby Redwood Color+Clear 6528502 134152 0112 9' Colorado Mountain Spruce Color+Clear 6528502 134394 0112 12' Colorado Mountain Spruce Color+Clear 6528502 216632 0112 7.5' Aspen Estate Fir Color+Clear 6528502 248622 0112 9' BH Fraser Fir™ Color+Clear 6528502 296214 0112 12' California Baby Redwood Color+Clear 6528502 307403 0112 12' BH Fraser Fir™ Color+Clear 6528502 363842 0112 9' Vermont White Spruce™ Narrow Color+Clear 6528502 364143 0112 10' Vermont White Spruce™ Color+Clear 6528502 364453 0112 11' Vermont White Spruce™ Color+Clear 6528502 364762 0112 10' BH Fraser Fir™ Color+Clear

CPSCFeb 28, 2013Nationwide• Redwood Pacific Ltd., of Hong Kong

Easy Go XP Lock Via Ferrata Lanyards (Singing Rock) – Mountain Climbing Risk (2013)

This recall involves Easy Go XP Lock Via Ferrata Lanyards used for shock absorption on Via Ferrata mountain climbing routes. The lanyard has two elasticized webbing branches with self-locking carabiners at each end. Recalled units can be identified by the elasticized webbing. "EASY GO XP LOCK" is printed on a white tag sewn into the zipper pouch.

CPSCFeb 27, 2013Nationwide• Singing Rock, of Ponikla, Czech Republic

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

Class IIILow

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

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

Class IIILow

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

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

Class IIILow

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

Monster High City Motor Scooter (Dynacraft) – Fall Hazard (2013)

This recall involves electric, battery-operated City Scooters that are purple and black with Monster High graphics on the front panels, seat and rear fenders. The scooters were manufactured between October 5, 2012 and November 7, 2012. Model number "8801-14" and the date of manufacture, formatted as "YYYY/MM/DD," are printed on a data label on the underside of the scooter's center platform. Serial numbers for the recalled scooters have the letters "QYCEI" followed by a six-digit number in the following range: 003125 through 014456. The serial number can be found etched on the underside of the scooter's center platform near the data label.

CPSCFeb 26, 2013Nationwide• Zhejiang Qunying Vehicle Co. Ltd., of China

Hello Kitty City Motor Scooter (Dynacraft) – Fall Hazard (2013)

This recall involves electric, battery-operated City Scooters that are pink and black with Hello Kitty graphics on the front panel, footboard and rear fenders. The scooters were manufactured between September 9, 2012 and December 3, 2012. Model number "8801-03" and the date of manufacture, formatted as "YYYY/MM/DD," are printed on a data label on the underside of the scooter's center platform. Serial numbers for the recalled scooters have the letters "QYCEI" followed by a six-digit number in the following range: 000001 through 014456. The serial number can be found etched on the underside of the scooter's center platform near the data label.

CPSCFeb 26, 2013Nationwide• Zhejiang Qunying Vehicle Co. Ltd., of China

Ryobi Lithium 18V Battery Pack (Techtronic) – Fire Hazard (2013)

Fire/Burn Risk

This recall involves Ryobi brand, Lithium 18 V 4Ah battery packs, with model P108 and part number 130429028. The battery pack is green, silver and black. "Ryobi" and "Lithium+18V" are printed in white lettering on both sides of the battery pack. The model and part number can be found on the data plate located on the bottom of the battery pack.

CPSCFeb 26, 2013Nationwide• Techtronic Industries (Dongguan) Co. Ltd. of China

Lisinopril Tablets (Mylan) – Incorrect Imprint (2013)

Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with an incorrect identifier code on the embossed tablets..

Class IIILow

FDAFeb 26, 2013Nationwide• Mylan Pharmaceuticals Inc.

Cefdinir Suspension (Teva) – Improper Seal (2013)

Defective Container: This recall is being carried out due to the potential for improperly sealed bottles.

Class IIModerate

FDAFeb 26, 2013Nationwide• Teva Pharmaceuticals USA, 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