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.
McKesson Medical-Surgical is recalling 26 cases of Cefazolin Sodium injection due to manufacturing deviations involving temperature abuse. The product was distributed nationwide.
GRUVIPA S.L. is recalling CB1102052 BOCATA ESPECIAL CASERO'S sandwiches distributed in Florida due to potential insect filth contamination. Consumers should not consume affected products.
Epinephrine injection vials are being recalled because they may have been exposed to improper temperatures during distribution, potentially affecting their effectiveness.
Centricity Enterprise Web medical imaging software may display inaccurate distance and area measurements when processing magnified or scaled images. The software is distributed to healthcare facilities worldwide.
McKesson Medical-Surgical is recalling 885 vials of Methylprednisolone Acetate Injectable Suspension USP (40 mg/mL) due to cGMP deviations from temperature abuse. The product was distributed nationwide, but specific lot numbers could not be identified by the distributor.
McKesson Medical-Surgical is recalling Xylocaine injectable vials nationwide due to temperature abuse during manufacturing and distribution. This local anesthetic is used for medical and dental procedures.
McKesson Medical-Surgical is recalling EpiPen Jr epinephrine auto-injectors nationwide due to temperature exposure during manufacturing that may degrade medication potency.
McKesson Medical-Surgical is recalling Methylprednisolone Acetate Injectable Suspension nationwide due to temperature abuse during manufacturing that may affect product quality. Healthcare providers should verify receipt.
Oakworks Inc is recalling PX200 Emergency Relief Beds due to labeling defects. The product label is missing the UDI number and states an incorrect weight capacity of 500 lbs instead of the actual 400 lb limit.
GE Healthcare's Centricity Universal Viewer Zero Footprint Client may display inaccurate distance and area measurements on magnified or scaled images.
The FDA is recalling 11 Getinge CM320 WUWD washer-disinfectors used for surgical instrument processing. Installation verification was not properly documented or completed, potentially creating risks of electrical shock, burns, and other injuries.
McKesson Medical-Surgical is recalling Albuterol Sulfate Inhalation Aerosol nationwide due to temperature abuse during distribution that may affect drug stability.
Intralipid intravenous fat emulsion is being recalled due to cGMP manufacturing deviations involving temperature abuse. The product was distributed nationwide.
McKesson Medical-Surgical recalled Cefazolin Sodium injectable (39 cases nationwide) due to temperature abuse during manufacturing that may compromise product sterility.
GRUVIPA S.L. is recalling CB1115007 Silvestre Cereales due to potential adulteration with insect filth. The recall affects 7,200 units distributed in Florida.
Trader Joe's Southwestern Chopped Salad is recalled because it contains an incorrect master pack with undeclared pistachio allergen. Consumers with pistachio allergies should not consume this product.
McKesson is recalling 55 packs of epinephrine auto-injectors nationwide due to temperature abuse during manufacturing. This represents a deviation from manufacturing standards.
McKesson Medical-Surgical is recalling Dexmedetomidine HCL single-dose vials due to temperature abuse during manufacturing or distribution that may have compromised product quality. No illnesses or injuries have been reported.
Kaufman is recalling 2018-2021 FXSG-10K-20D and FXSG-10K-20D-SC trailers because insufficient welds on the ramp holding bracket may allow the ramp to fall, increasing injury risk.
Kentucky Trailer Manufacturing is recalling 2014-2021 MV and PV trailers because walk board rack bolts may loosen, allowing the rack to separate and fall.
Shyft Group is recalling 2021-2022 Utilimaster Walk-In Vans because the passenger-side jump seat headrest may be installed incorrectly, increasing injury risk in a crash.
Nova Bus is recalling 2019-2022 LFS and LFS Artic buses because a corroded fuse holder may cause an electrical short, increasing the risk of a fire.
Ford is recalling 2021-2022 Bronco four-door vehicles because the passenger-side rear door can open from inside the vehicle when the child safety lock is in the "ON" position, increasing the risk of injury to child occupants.
Ford is recalling 2013-2021 Transit Connect vehicles because the shifter cable bushing may degrade and prevent intended gear selection. This can cause unintended vehicle movement or rollaway after selecting Park, increasing crash and injury risk.
Ford is recalling 2022 Transit vehicles because the instrument panel cluster may fail to illuminate gauges and telltales, potentially increasing crash risk.