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.
Cook Inc. is recalling two Pericardiocentesis Catheter Trays because the catheter distal end hole may be too small. The affected units were distributed domestically and internationally.
Flowonix Medical Inc is recalling 40 units of Prometra Programmer software due to a defect that causes intrathecal pumps to shut down unexpectedly.
Zimmer Biomet is recalling 11 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw material was used, potentially leading to corrosion.
AngioDynamics is recalling 7,348 Solero Microwave Tissue Ablation applicators to update manuals and software, reducing the risk of patient harm from procedure delays.
Godwin is recalling 2017 dump bodies equipped with Whelen brake lights that may illuminate without the brake pedal being pressed, potentially confusing other drivers.
LA West is recalling 2018-2019 Ford Transit vehicles with modified glass roof hatches that may shatter due to stress, posing an injury risk.
Vac-Tron is recalling 2015-2019 LP 873 SD trailers that may lack required lights and reflectors, increasing crash risk at night.
Unicell is recalling 325 commercial vehicles equipped with ASA Electronics Voyager monitors that may display reversed back-up camera images, increasing crash risk.
Amazon is recalling AmazonBasics 1500 Watt Ceramic Space Heaters because they can overheat, posing fire and burn hazards. Consumers should stop using the heaters and contact Amazon for a full refund.
Target is recalling Cat & Jack 'Lilia' toddler rain boots because the unicorn horn can detach, posing a choking hazard to young children.
Entegra is recalling 2020 Anthem and Cornerstone motorhomes because an insufficiently tightened steering shaft bolt may cause steering failure, increasing crash risk.
Cushy Form is recalling about 2,300 folding mattresses sold on Amazon.com because they fail to meet federal flammability standards, posing a fire hazard.
Chrysler is recalling 2019 Jeep Renegade vehicles with the Upland trim package because the occupant restraint controller may be miscalibrated, increasing injury risk in crashes.
Forest River is recalling 2011-2017 Glaval Universal transit buses because they are missing required emergency egress windows, which could trap occupants in an emergency.
Mickey Truck Bodies is recalling 2017-2018 Ford F-750 vehicles because back-up camera monitors may revert to factory settings, causing the image to reverse and increasing crash risk.
Newmar is recalling specific 2016-2019 motorhomes because a damaged power module may cause rear lights to fail, increasing crash risk.
Morgan Olson is recalling 2018 P31 vehicles because backup camera monitors may revert to factory settings, causing the image to reverse and increasing crash risk.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because a fuse failure may reduce driver visibility, increasing crash risk.
SkyMark Refuelers is recalling 2018 Flowmark Vacuum Trucks because the back-up camera monitors may revert to factory settings, reversing the image and increasing crash risk.
Life Line Emergency Vehicles is recalling 2017-2018 Type I ambulances because the back-up camera image may reverse, increasing the risk of a crash.
Diamond Coach is recalling one 2017 VIP 2800 vehicle because the backup camera display may revert to factory settings, causing the image to reverse and increasing crash risk.
Maquet Cardiovascular is recalling Pediatric ECC Packs because a design feature may prevent sterilization gas from reaching all fluid paths, compromising sterility.
Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design flaw may prevent proper sterilization of stopcock ports.
Suja Life LLC is recalling 66,964 bottles of Organic Kombucha - Mixed Berries because consumers reported finding pieces of glass in the product.
Suja Life LLC is recalling 31,079 cases of Organic Kombucha Variety Packs because consumers reported finding pieces of glass in the bottles.