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All product recalls associated with Seabear Company.
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.
Potential for growth of C. botulinum
Undeclared Allergen
Forest River, Inc. (Forest River) is recalling certain 2021-2022 Coachmen Nova motorhomes. The Absorbed Glass Mat (AGM) battery was incorrectly installed inside the vehicle, which can allow hydrogen gas to enter the vehicle.
The devices malfunction under specific operator workflows.
CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
False Mutation Detected results for the exon 20 insertion (Ex20Ins) mutation when using the cobas EGFR Mutation Test v2, may lead to inappropriate treatment
CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Failed Impurities/Degradation Specifications
There is a potential for false positive results.
Engraving on implants may not match what is listed on the pouch labels.
There is a potential for false positive results.
Engraving on implants may not match what is listed on the pouch labels.
Subpotent Drug
Stability is out of spec at 81% for 3 month time period.
There is a potential for false positive results.
Subpotent Drug
Labeling: Incorrect Instructions
Subpotency: one product for active ingredient assay and another one for preservative assay
Subpotency: one product for active ingredient assay and another one for preservative assay