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.
Aesculap Implant Systems is recalling PRESTIGE ATRAUMATIC GRASPER surgical instruments because the weld connecting the handle to the shaft may separate during use.
United Natural Foods, Inc. is recalling Grandpa's brand yogurt muffins sold in Alabama and Mississippi due to temperature abuse during delivery to retail stores. No illnesses have been reported.
United Natural Foods, Inc. recalls frozen deli salads and prepared foods distributed in Alabama and Mississippi due to temperature abuse during delivery to retail stores.
Teva Pharmaceuticals is recalling Matzim LA (Diltiazem Hydrochloride) 180 mg tablets because they failed to meet dissolution specifications. The recall affects approximately 8,022 bottles distributed nationwide in the United States and Puerto Rico.
Altec Industries is recalling 2015-2022 DT65 and DT85 Aerial Devices because a weld crack could cause the auger bracket to detach, increasing injury risk.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Nighttime due to manufacturing without an approved acidification process. The product's preservation safety cannot be assured.
United Natural Foods, Inc. is recalling multiple brands of frozen prepared foods distributed to retail stores in Alabama and Mississippi due to temperature abuse during delivery. The temperature-abused foods may have been exposed to unsafe conditions allowing bacterial growth.
Multiple frozen seafood products from various brands distributed in Alabama and Mississippi were recalled due to temperature abuse during delivery to retail stores. No illnesses have been reported.
Intuitive Surgical is recalling 505 E-100 electrosurgical generators because required preventative maintenance was not performed on units distributed worldwide and in the US.
St. Jude Medical recalls Merlin 2 PCS model MER3700, software used to program and interrogate Abbott implantable medical devices.
Ragozzino Foods is recalling Creamy Parmesan Risotto distributed in New York, Florida, Illinois, and California due to potential glass contamination. Consumers should not eat the affected product.
United Natural Foods, Inc. is recalling multiple brands of frozen vegetable products distributed in Alabama and Mississippi due to temperature abuse during delivery to retail stores.
St. Jude Medical recalled Merlin 2 PCS MER3400 programmer software version 1.1.2 revision 1 or earlier in an FDA Class II recall. The recall affects 622 units distributed across the United States and internationally.
Navistar is recalling 2023 International and IC Bus commercial vehicles because the engine control module may short-circuit, causing the engine to stall unexpectedly. This defect increases the risk of crashes.
Pleasure Way is recalling 2021–2022 Rekon, Tofino, Ascent, Plateau, and Ontour motorhomes due to a mislabeled DCF4 circuit board. The board is labeled for 30 amps but has pins rated for only 20 amps, creating a fire risk.
Food trailers experienced temperature control failures while transporting frozen food products to retail stores in Alabama and Mississippi. The products experienced temperature abuse that could affect food safety.
St. Jude Medical's Merlin PCS 3650 programmer software may display overestimated predicted battery longevity for certain pacemakers. This could affect clinical decision-making regarding device maintenance and replacement timing.
Refrigerated dressings sold under Cindy's and Bolthouse brands from United Natural Foods, Inc. are being recalled due to temperature abuse during delivery to stores in Alabama and Mississippi.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Daytime dietary supplement due to use of an unapproved acidification process. The product was distributed to 42 states in approximately 34,526 cases.
Craftmatic Industries is recalling the Model 1 Base for Dual Bed Configurations due to a potential for the bed bases to separate or slip apart. This defect could cause dual-configured beds to shift unexpectedly.
Natural Grocers Amaranth Grain has been recalled due to potential Salmonella contamination. The FDA Class II recall affects 6,351 units distributed across 21 states.
Dental Choice is recalling 708 units of the CustMbite Model CBT-SRS-UL device nationwide because it was marketed and sold without FDA clearance.
Craftmatic Industries recalls the Legacy Base for Dual Bed Configurations due to a potential for beds to separate or slip away from one another. The defect poses a risk of unintended bed movement.
Thor Motor Coach is recalling 2022-2023 motorhomes whose electric retractable awning may drop due to a failing welded seam. This increases the risk of injury.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Combo Pack because the acidified/low acid dietary supplement was manufactured without an FDA-approved process.