Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Philips is recalling UroDiagnost x-ray systems because bolts may break, causing the c-arm to move and sag.
Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts attaching the clamping plate may break, causing the C-arm to sag.
Stryker Medical is voluntarily recalling Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.
Zimmer Biomet is voluntarily recalling 169 V-TEK Twist Drills because a potential tolerance stack-up was identified between the drill and the mating Kirschner Wire component.
NeoCoil, LLC is recalling 39 units of the 3T 16ch Flex SPEEDER Large Coil due to a potential for higher than specified surface temperatures.
Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts may break, causing the C-arm to sag. The recall covers units distributed worldwide.
Philips is recalling IntelliVue Patient Monitors because they may display outdated waveform data if powered on continuously for several months, failing to reflect current patient conditions.
Zimmer Biomet is voluntarily recalling 169 Twist Drills because a potential tolerance stack up was identified between the drill and the mating Kirschner Wire component.
Stryker Medical is voluntarily recalling Spirit Select and Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.
Moller Vital is recalling Molift Air ceiling hoists because the suspension coupling bolt may come loose, posing a risk of patient falls.
Stryker is recalling Trident Constrained Liner Inserter Impactor Tips because they do not meet required sterility assurance levels when steam sterilized.
GE Inspection Technologies is recalling four Phoenix v|tome|x m240 cabinet x-ray systems because radiation emissions exceeded safety limits due to insufficient door shielding.
BD is recalling specific Diamond-Flex Circular Retractors because a weld failure could cause wire protrusion, potentially damaging tissue or organs during use.
Sunrise Medical is recalling Quickie Q7 wheelchairs because the backrest bracket can fracture, causing the backrest to detach from the chair frame.
Elekta is recalling 383 units of the MOSAIQ Oncology Information System because a software issue may prevent order changes from saving, potentially resulting in incorrect chemotherapy doses.
Ortho-Clinical Diagnostics is recalling VITROS Calcium Slides due to potential negatively biased results that may affect diagnosis.
The Metrix Company is recalling container fill and transfer sets because they cannot meet designed accuracy specifications when dispensing into bags.
The Metrix Company is recalling 16 AUTOCOMP6 XPS High Speed Compounders because they cannot meet designed accuracy specifications when dispensing into bags.
Ge Healthcare is recalling Imagecast PACS software versions prior to 10.6 Update Package 18 because a defect causes images to be out of context with clinical information.
The Metrix Company is recalling container fill and transfer sets because they may not meet designed accuracy specifications when dispensing into bags.
The Metrix Company is recalling 93 AUTOCOMP6 XP High Speed Compounders because they cannot meet designed accuracy specifications when dispensing into bags.
Integra LifeSciences Corp. is recalling 27 units of the External Fixation System Rocker Bottom because the embedded silicone insert may become dislodged or loose.
Zimmer GmbH is recalling two Avenir Moller hip stem models due to a packaging mix-up that could lead to the use of the incorrect implant.
Beckman Coulter is recalling Allegra X-5 rotor yokes because a defect allows improper rotor seating, which could lead to rotor failure if buckets are loaded in an imbalanced configuration.
Draeger Medical is recalling 1,599 Babytherm infant warmers due to a risk associated with operating the device in skin temperature mode without a patient connected.