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All product recalls associated with INTERNATIONAL.
Total Recalls
1000
Past Year
135
Class I (Serious)
159
Most Recent
Dec 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.
Navistar, Inc. (Navistar) is recalling certain 2020 International HV 6X4 vehicles. The vehicles were built with a non-Quick Release Modulator Valve (NQRMV) instead of a Quick Release Modulator Valve (QRMV), which may affect the brake release time. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 121, "Air Brake Systems."
This recall involves Cutek Proclean Professional Wood Restoration. The product was sold in a clear plastic one-gallon bottle with a blue, black and white label. "Cutek Proclean Professional Wood Restoration" is printed on the front of the product and UPC 098411800166 is printed on the side panel of the product.
Potential leak in the balloon extension line. If a leak was present and went undetected during pre-use testing as outlined in the IFU, this would cause the balloon to deflate slowly following placement. If the leak went undetected by attending clinicians during use, it could result in contrast injection into the vascular or cardiac tissue which could result in serious injury or death
Potential to be contaminated with Listeria monocytogenes
Potential to be contaminated with Listeria monocytogenes
Potential to be contaminated with Listeria monocytogenes
Product contains undeclared sulfites.
Direct Account randomly tested two products with presumptive positive results for Listeria monocytogenes.
Direct Account randomly tested two products with presumptive positive results for Listeria monocytogenes.
Direct Account randomly tested two products with presumptive positive results for Listeria monocytogenes.
Direct Account randomly tested two products with presumptive positive results for Listeria monocytogenes.
Product contains undeclared sulfites
The firm initiated the recall due to incorrect information on the label. The product label lists an incorrect manufacturer number, pack date, and expiration date.
Undeclared sulfites.
Notified by customer of reports of illness after consuming tuna steaks, found high levels of histamines.
Product may be contaminated with Listeria monocytogenes
Alfa International Seafood Inc. was notified by Kroger retail stores of complaints from consumers who experienced symptoms of scombroid poisoning after eating yellowfin tuna steaks supplied by Alfa International Seafood Inc.
Borosilicate glass material found in FDA Sample.
FDA refused product due to Salmonella were mistakenly distributed to a retail supermarket.
Products may contain the incorrect banner card within the kit