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All product recalls associated with H E B.
Total Recalls
1000
Past Year
198
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.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
Use of ingredient with violative pesticide residue.
The recall involves adult portable bed handles that do not have safety retention straps to secure the bed handle to the bed frame to keep the bed handle from shifting out of place and creating a dangerous gap. Recalled models include the Original Bedside Assistant® (BA10W), the Travel Handles™ (BA11W) which is sold as a set of two bed handles, and the Adjustable Bedside Assistant® (AJ1). The L-shaped bed handles are made out of ¾ inch tubular steel, measure 20 inches wide, 16 to 20 inches tall and have 3 ft. poles that extend under the mattress. The Original Bedside Assistant® (BA10W) and the Travel Handles™ (BA11W) have a white handle with white poles that go under the mattress. The Adjustable Bedside Assistant® (AJ1) is gold in color and has a black cushioned foam handle. The bed handles are intended to assist adults with getting in and out of bed by giving them a bar to grip. Bed Handles, Inc. and the model number are printed on a white label on the bed handles.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.