Recalls

All US Product 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.

How to read this listing

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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

18776–18800 of 27647

HighFDA (Devices)·Z-0502-2018·2018-02-07
Beaver Xstar Safety Slit Knives Recalled Due to Retracted Protective Shield
Beaver-Visitec International Inc. is recalling 659,370 units of bvi Beaver Xstar Safety Slit Knives because the protective shield was retracted, exposing the blade.
Product
bvi Beaver Xstar Safety Slit Knife: (a) REF 378214, 1.4mm, 45o Bevel Up (b) REF 378215, 1.50mm, 45o Bevel Up (c) REF 378217, 1.7mm, 45o Bevel Up (d) REF 378218, 1.8mm, 45o Bevel Up (e) REF 378220, 2.0mm, 45o Bevel Up (f) REF 378222, 2.2mm, 45o Bevel Up (g) REF 378223…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0459-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may not be in the correct location, potentially preventing proper product assembly.
Product
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 420MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, preventing proper product assembly.
Product
Affixus Hip Fracture Nail, RH 125 DEG 13MM X 320MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0493-2018·2018-02-07
Horiba Medical Recalls ABX PENTRA Reagent Cups Due to Fit Issues
Horiba Medical is recalling ABX PENTRA reagent cups that may not sit properly in the rack, potentially causing incorrect test results without an alarm.
Product
10 ML REAGENT CUP, B1034626, SAP 1221034626 for use with ABX PENTRA 400 / PENTRA C400
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0413-2018·2018-02-07
Ormco/Sybronendo Recalls Elements Obturation Units and Buchanan Heat Pluggers
Ormco/Sybronendo is recalling 25,765 Elements Obturation Units and Buchanan Heat Pluggers because the pluggers may overheat during use.
Product
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger. It is intended to be used in Dentistry to provide continuous heat at the tip of a dental instrument to test tooth response to thermal stimulus, for tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0465-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 320MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0436-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 400MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0485-2018·2018-02-07
Baxter Recalls 500mL IntraVia Containers Due to Potential Sterility Leak
Baxter Healthcare is recalling 29,088 units of 500mL IntraVia containers in the US and Canada because a leak may allow microbial contamination of the sterile fluid path.
Product
Empty IntraVia Container with Non-DEHP Fluid Path, 500mL Containers are intended for use in the preparation and administration of drug admixtures.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0435-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent the device from being properly assembled.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 380MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent the set screw and sleeve assembly from staying in place.
Product
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 380MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0479-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, preventing proper product assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 340MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 280MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0463-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 280MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0500-2018·2018-02-07
Beaver-Visitec Recalls Safety Knives Due to Retracted Protective Shield
Beaver-Visitec International Inc. is recalling specific EdgeAhead Safety Knives because the protective shield retracted, exposing the blade.
Product
bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR .90mm 20G, REF 370531 (b) Sideport Angled, .60mm (23G), REF 378233 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0476-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 260MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0478-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 320MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0494-2018·2018-02-07
Horiba Medical Recalls ABX PENTRA Reagent Cups for Fit Issues
Horiba Medical is recalling 15 mL reagent cups for ABX PENTRA analyzers because they may not sit properly in the rack, potentially causing incorrect test results without an alarm.
Product
15 ML REAGENT CUP, B1037307, SAP 1221037307 for use with ABX PENTRA 400 / PENTRA C400
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0412-2018·2018-02-07
MicroAire Recalls Sterile Twist Drills Due to Incorrect Size Inclusion
MicroAire Surgical Instruments is recalling 42 sterile twist drills because one lot contained an incorrect 2.0mm drill alongside the correct 1.6mm drill.
Product
SST TWIST DRILL, STANDARD, 1.6mm Dia. x 127mm, REF 8054-010, STERILE This product line is intended for use in orthopaedic surgery (large and small bone surgeries) to cut bone
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0487-2018·2018-02-07
GE Healthcare CARESCAPE Central Station software recall for communication issues
GE Healthcare is recalling CARESCAPE Central Station software version 2.0.2 because units may experience unexpected network communication issues after boot-up or restart.
Product
GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and/or other non-medical information.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0438-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0433-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 300MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0426-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0484-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of the Affixus Hip Fracture Nail because a manufacturing rework error may have displaced internal components, preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 360MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0467-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 360MM
Category
Medical Device
Distribution
Distributed nationwide

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18776–18800 of 27647