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All product recalls associated with COOPER.
Total Recalls
128
Past Year
22
Class I (Serious)
18
Most Recent
Aug 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.
Goodyear Tire & Rubber Company (Goodyear) is recalling certain Cooper Discoverer Stronghold AT tires, size LT275/65R18. The tire identification number (TIN) is missing the 4-digit week and year code mark. As such, these tires fail to comply with the requirements of Federal Motor Vehicle Safety Standard Number 574, "Tire Identification & Recordkeeping."
a limited number of lots were manufactured with an incorrect cylinder power.
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
Cheese curds may be contaminated with generic E. coli.
Cheese curds may be contaminated with generic E. coli.
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
During the manufacturing process the devices were laser-marked with the incorrect part number.
During the manufacturing process the devices were laser-marked with the incorrect part number.
Low concentration of sodium pyruvate in the wash could compromise gamete development
The firm has become aware of a sudden increase in complaints for three associated lots. Performance issues may lead to impaired embryo development prior to the blastocyst stage.
Incorrect component descriptions within the "Contents" section on the Tyvek lid for individual kit trays.
Cheese may be contaminated with Listeria monocytogenes.
The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
It has come to CooperSurgical's attention that the affected Product may contain a medium other than the Global Total LP single step medium which does not contain the protein source required for embryo culture and development.
Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
The affected product may contain a medium other than the Biopsy Medium. There is a risk that use of the Product from this lot could cause degradation of the embryo.
Firm has received 11 complaints involving a loose or detached metal clips, including 3 cases where the metal clip was ingested by the patient, and 3 cases where the metal clip was removed from the patient's mouth. In one case, the patient suffered a laceration to the throat.