Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Bakkavor USA is recalling 16-ounce Savory Tuna Salad containers distributed in Texas because the product contains undeclared shrimp.
Zimmer Biomet is recalling 384 units of the XP-XP Tibial Tray - Interlok 83 mm because the locking bar may not fully engage.
Stryker is recalling 946 Berchtold Chromophare F528 surgical lights because the back cover of the light head was insufficiently assembled and could fall off.
Stryker is recalling 3,344 Berchtold Chromophare F628 surgical lights because the back cover of the light head was insufficiently assembled and could fall off.
Zimmer Biomet is recalling 82 units of the XP-CR Tibial Tray because the locking bar may not fully engage.
Aesculap Implant Systems LLC is recalling Caiman disposable articulated instruments due to a possibility of insufficient sterilization.
Bubbies is recalling Mochi Ice Cream and related products due to potential foreign plastic pieces. The recall covers 3.4 million cases distributed nationwide and internationally.
Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.
Instrumentation Laboratory is recalling 364 ROTEM ex-tem kits because they may produce prolonged clotting times. The recall affects specific lots distributed in the US and internationally.
Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces.
Zimmer Biomet is recalling 454 units of XP-CR Tibial Trays because the locking bar may not fully engage.
Zimmer Biomet is recalling 50 units of the XP-XP Tibial Tray - Interlok 59 mm because the locking bar may not fully engage.
Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.
Bubbies Mochi Ice Cream is being recalled due to the potential for free-floating foreign plastic pieces in the product.
Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vehicles because head restraint spring pins may be missing or improperly mounted, increasing injury risk in a crash.
Zimmer Biomet is recalling Vanguard XP Tibial Trays because the locking bar may not fully engage. The recall covers units distributed in the US and internationally.
Bubbies is recalling Mochi Ice Cream and Cookie Dough Ice Cream Bites due to the potential for free-floating foreign plastic pieces in the product.
Bubbies is recalling Mochi Ice Cream and Cookie Dough Ice Cream Bites due to potential foreign plastic pieces.
Zimmer Biomet is recalling 973 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Compounded Solutions in Pharmacy is recalling 20% Acetyl-L-Cysteine Ophthalmic Solutions because of a lack of processing controls. The product was dispensed to patients in 3ml dropper bottles.
Great One Trading Inc. is recalling QQ Fish brand Shrimp Flavoured Seafood Balls because they contain an undeclared egg allergen.
Zimmer Biomet is recalling 1,282 units of the XP-XP Tibial Tray because the locking bar may not fully engage.
Zimmer Biomet is recalling 369 units of the XP-CR Tibial Tray - Interlok 75mm because the locking bar may not fully engage.
Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces in the product.
Zimmer Biomet is recalling 84 units of Vanguard XP Tibial Tray 73 mm because the locking bar may not fully engage.