The Recall Desk

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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

20776–20800 of 40248

  • ModerateFDA (Devices)·Z-1390-2019·2019-05-29

    Thommen Medical Recalls Dental Adapters for Handpiece Due to Deformation Risk

    Thommen Medical AG is recalling 15 units of dental adapters for handpieces because the coupling may deform, making removal difficult.

    Product
    Adapter for handpiece, guided, reusable, for guide sleeve 0 4.8 mm Article number: 3.04.090 - Product Usage: The adapter for handpiece, guided reusable, for guide sleeve ¿ 4.8 mm is used to transfer the implant from the packaging to the patient via a plug-in connection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1444-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling specific cannulated drills because an investigation found they may have been manufactured from a different material than defined in specifications.

    Product
    Drill, cannulated, 3x90mm, AO, Item Number 502015631
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1452-2019·2019-05-29

    Zimmer GmbH Recalls Contra-Angle Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling contra-angle drills that may have been manufactured from a different material than specified. The products were distributed to 41 US states.

    Product
    Drill, contra-angle, 1.5x85mm, Item Number 502015706
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1367-2019·2019-05-29

    CooperSurgical Recalls ICSI Micropipettes Due to Missing Bend

    CooperSurgical is recalling 480 ICSI Micropipettes because the required thirty-degree bend is absent. The affected units were distributed in Denmark, Italy, and Sweden.

    Product
    ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1378-2019·2019-05-29

    Remel Inc Recalls Thio Med w/Dex, Hemin, Vit K Media

    Remel Inc is recalling Thio Med w/Dex, Hemin, Vit K media because the products may fail performance testing after 57 days.

    Product
    Thio Med w/Dex, Hemin, Vit K (5ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1399-2019·2019-05-29

    Boston Scientific Recalls Auriga 30 Laser Systems Due to Power Degradation

    Boston Scientific is recalling two Auriga 30 laser systems because a mechanical cooling issue may cause faster-than-normal power degradation and a low power error.

    Product
    AURIGA 30 GENERAL ZERO COST SYSTEM UPN: M0068S30GZ0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber optic delivery system is intended to be used in surgical procedures such as open, laparoscopic and endoscopic, to perform…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1482-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation

    Zimmer GmbH is recalling specific cannulated drills that may have been manufactured from a material different from the defined specifications.

    Product
    Drill, cannulated, 3x90mm, AO, Item Number ST502015631
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1417-2019·2019-05-29

    Stryker 26mm Drill Recalled for Potential Material Specification Deviation

    Zimmer GmbH is recalling Stryker 26mm drills because an investigation found they may have been manufactured from a different material than specified.

    Product
    Drill, 26mm stop, 1.4x94mm, Stryker, Item Number 502015120
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1398-2019·2019-05-29

    Boston Scientific Recalls Auriga 30 Laser Systems Due to Power Degradation

    Boston Scientific is recalling specific Auriga 30 laser systems because a mechanical cooling issue may cause faster-than-normal power degradation and low power errors.

    Product
    AURIGA 30 GENERAL - DEMO SYSTEM UPN: M0068S30GD0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber optic delivery system is intended to be used in surgical procedures such as open, laparoscopic and endoscopic, to perform…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1402-2019·2019-05-29

    Remel Thio Med Culture Media Recalled for Potential Performance Failure

    Remel Inc is recalling Thio Med culture media due to potential failure to meet performance standards after 106 days from manufacturing.

    Product
    Thio Med w/o Ind, w/Dex (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1428-2019·2019-05-29

    Zimmer GmbH Recalls 2.7mm AO Surgical Drills Due to Material Concerns

    Zimmer GmbH is recalling specific 2.7mm AO surgical drills because they may have been manufactured from a material different from the specifications.

    Product
    Drill for 2.7mm screw, 2x100mm, AO, Item Number 502015208
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1394-2019·2019-05-29

    Boston Scientific Recalls Auriga XL 4007 Laser Systems for Cooling Defect

    Boston Scientific is recalling six Auriga XL 4007 laser systems worldwide due to a mechanical cooling issue that may cause power degradation and stop laser emission.

    Product
    AURIGA XL 4007 GENERAL - ZERO COST SYSTE UPN: FS4007GZ0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber optic delivery system is intended to be used in surgical procedures such as open, laparoscopic and endoscopic, to…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1465-2019·2019-05-29

    Zimmer GmbH Recalls V-TEK Micro-countersink Due to Material Concerns

    Zimmer GmbH is recalling V-TEK Micro-countersink items because they may have been manufactured from a different material than specified.

    Product
    V-TEK", Micro-countersink, AO, Item Number 28.66.113
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1436-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the applicable specifications.

    Product
    Drill, cannulated, 4x150mm, AO, Item Number 502015403
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1445-2019·2019-05-29

    Zimmer V-TEK IVP Step Drill Recalled for Material Specification Deviation

    Zimmer GmbH is recalling V-TEK IVP step drills because they may have been manufactured from a different material than specified.

    Product
    V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, contra-angle, Item Number 502015634
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1437-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.

    Product
    Drill, cannulated, 2x95mm, round shaft, Item Number 502015619
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1403-2019·2019-05-29

    Remel Thio Med w/Dex, Hem, Vit K Media Recalled for Performance Failure

    Remel Inc is recalling Thio Med w/Dex, Hem, Vit K media because it may fail performance testing after 106 days. The expiration date is being shortened from 9 months to 105 days.

    Product
    Thio Med w/Dex, Hem, Vit K (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1401-2019·2019-05-29

    Remel Thio Med w/Dex, Hem, Vit K Media Recall for Performance Failure

    Remel Inc is recalling Thio Med w/Dex, Hem, Vit K media because products may fail performance testing after 106 days from manufacturing.

    Product
    Thio Med w/Dex, Hem, Vit K (9ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1421-2019·2019-05-29

    Stryker 2.5x94mm Drill Recalled for Potential Material Deviation

    Zimmer GmbH is recalling Stryker 2.5x94mm Drills because an investigation found they may have been manufactured from a different material than specified.

    Product
    Drill, 2.5x94mm, Stryker, Item Number 502015136
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1483-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation

    Zimmer GmbH is recalling specific cannulated drills that may have been manufactured from a material different from the defined specifications.

    Product
    Drill, cannulated, 3.5x90mm, round shaft, Item Number ST502015635
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1391-2019·2019-05-29

    Boston Scientific Recalls Auriga XL 4007 Laser System for Cooling Defect

    Boston Scientific is recalling specific Auriga XL 4007 laser systems due to a mechanical cooling issue that may cause premature power degradation and low power errors.

    Product
    AURIGA XL 4007 BRAZIL SYSTEM Model: M0068FS4007B0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber optic delivery system is intended to be used in surgical procedures such as open, laparoscopic and endoscopic, to perform…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1438-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications.

    Product
    Drill, cannulated, 2.5x95mm, round shaft, Item Number 502015620
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1281-2019·2019-05-29

    NeuViz 16 Essence CT Scanner Recalled for Software Defect

    Neusoft Medical Systems is recalling two NeuViz 16 Essence CT scanners due to a software defect that may cause image loss during specific scans.

    Product
    NeuViz 16 Essence Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray system featuring a continuously rotating x-ray tube and detector array. The acquired x-ray transmission data is…
    Category
    Medical Device
    Distribution
    Distributed nationwide