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.
Prevost is recalling 682 model year 2012-2014 motorhomes and coaches because a windshield wiper motor housing may crack, causing loss of wiper function and reduced visibility.
Senor Murphy Candymaker is recalling eight types of candy products because they contain undeclared allergens.
Baxter is voluntarily correcting ABACUS TPN software versions 2.0-3.0 because data corruption could cause patients to receive another patient's TPN order.
Remel Inc. is recalling 109 kits of Streptex Latex D reagent because the product may produce weak or false negative test results for streptococcal group D.
GE OEC Medical Systems is recalling InstaTrak and ENTrak navigation systems due to potential safety issues.
Garden-Fresh Foods is recalling various cut vegetables, ready-to-eat salads, and dips manufactured before November 6, 2013, due to potential Listeria monocytogenes contamination.
Taylor Farms is recalling Broccoli Crunch Kits because the included salad dressing was recalled for possible Listeria monocytogenes contamination.
Turkey Hill is voluntarily recalling Moose Tracks frozen dairy dessert due to potential metal debris contamination.
Intuitive Surgical is recalling Mega Needle Drivers for the da Vinci S and Si systems due to a potential risk of jaw insert detachment.
Global Health Laboratories is recalling UT-Fem FOR WOMEN dietary supplements contaminated with chloramphenicol, an antibiotic, at levels above 0.3 ppb.
Turkey Hill Dairy is voluntarily recalling 756 tubs of Pumpkin Pie Premium Ice Cream due to potential metal debris contamination.
Senor Murphy Candymaker is recalling Chocolate Pretzels and other confections due to undeclared allergens. Consumers should stop using the products.
Garden-Fresh Foods is recalling various cut vegetables, ready-to-eat salads, slaw, spread, and dip products manufactured prior to November 6, 2013, due to potential Listeria monocytogenes contamination.
ASI Medical is recalling 337 SEAC Advanced Dental Systems because the miniature plastic air tank can potentially rupture.
Garden-Fresh Foods is recalling various cut vegetables, ready-to-eat salads, slaw, spread, and dip products manufactured prior to November 6, 2013, due to potential Listeria monocytogenes contamination.
Garden-Fresh Foods is recalling specific lots of Grandpa's and Our Own fresh salsa because they may be contaminated with Listeria monocytogenes.
Taylor Farms is recalling Broccoli Slaw Kits because they contained salad dressing from Reser's that was recalled for possible Listeria monocytogenes contamination.
Roche Diagnostics is recalling 27 MagNA Pure 96 Systems due to a software issue that may cause sample mismatches when importing XML files.
Qualigen Inc is recalling six FastPack immunoassay kits because a manufacturing defect may cause lower than expected test results.
Senor Murphy Candymaker is recalling eight candy products due to undeclared allergens. Consumers should stop eating these items and check the recall list.
Taylor Farms Tennessee is recalling six Giardiniera Vegetable Salad Kits because the included dressing may be contaminated with Listeria monocytogenes.
Mobility Unlimited Inc. is recalling 33 KayserBetten model IDA beds because door joints may loosen or separate, causing doors to drop outward and potentially injure users.
Siemens is recalling Dimension TACR Flex reagent cartridges because reduced stability may cause inaccurate test results for transplant patients.
Senor Murphy Candymaker is recalling eight confection products due to undeclared allergens. Consumers should stop eating these items and return them to the point of purchase.
Intuitive Surgical is recalling Large Needle Drivers for the da Vinci S and Si systems because the jaw insert may detach during use.