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All product recalls associated with Cook, Inc..
Total Recalls
1000
Past Year
731
Class I (Serious)
175
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.
Packaging Problem: The peel-away sheath does not peel uniformly or completely.
Packaging Problem: The peel-away sheath does not peel uniformly or completely.
The recalled holiday figurines are painted plastic snowmen and bears. The SKU number is printed on the bottom of the product. Product Size SKU Number Holiday Bear Door Greeter 17" x 16" 894-825 Snowman with "Let it Snow" Sign Tabletop item 894-893 Three Snowmen with "Joy" Sign 13" x 17" 898-964 Snowman Votive Holder 7.5" x 7.5" 967-467
Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.
Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.
Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.
In vitro diagnostic test reagent for identification of Shigella bacteria in patient samples may cause false negative results.
In vitro diagnostic test reagent for identification of Shigella bacteria in patient samples may cause false negative results.
Marketed without a 510(k)
This recall involves the Lazy Lounger chair (Style # CEH00415), recliner (Style # CEH00320) and oversize recliner (Style # CEH00414, CEH00345, and CEH00443). Style numbers are printed on the packaging. The chairs have a mesh covering that attaches to a black or tan metal frame by a woven cord. The mesh covering is sold in: blue, orange, black, natural, burgundy, pink, white, green, red, khaki, and camouflage. A padded headrest pillow is sewn on to the mesh. Beneath the padded headrest are two tags. The first reads: "! WARNING !", followed by 9 numbered statements, and "Made in China". The second is the "Do Not Remove Under Penalty of Law" tag and includes the manufacturer's Registration No: OHIO36462HK.
Marketed without 510(k)
The recalled necklace and earring sets have a silver metal chain and a round pendant with a light blue jewel and three jeweled dangling charms.
Safety Mechanism Failure: the safety mechanism of the BD Vacutainer Push Button Collection Set with Pre-attached holder cannot be activated; thus the needle cannot retract into the rear barrel.
No Fluid Flow or Restricted Fluid Flow: Nucleus Hydrodissector(s) were found to have reduced or no fluid flow.
Cannot connect: Tips have electrodes that are too large to fit monopolar cables and are unusable.
Mislabeling: incorrect control range-The Level 1 control solution range printed on the 50-count test strip bottles is incorrect. The range printed on the bottle is 62-54 when it should be 62-94.
Curvature Discrepancy -- The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants.
Delamination: Loosening of the titanium plasma coating on the product was observed on twelve non-distributed units.
The recalled football helmet chin strap consists of a plastic cup with a foam liner, straps and four metal snaps. They were sold in both youth and adult sizes and come in black/gray and white/gray color combinations. The Nike Swoosh trademark is printed on the outside of the chin cup and DRI-FIT™ is printed on the foam liner. "Made in China" and one of the following four style numbers is printed on the inside of the strap: FA0016 046, FA0016 130, FA0021 046, or FA0021 130.
Power supply reliability: McKesson received word from their manufacturer of the medical grade power supply that some power grade supplies may not provide reliable power output.