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

15976–16000 of 27471

  • HighFDA (Devices)·Z-1392-2019·2019-05-29

    Boston Scientific Recalls Auriga XL 4007 Laser Systems for Cooling Defect

    Boston Scientific is recalling 27 Auriga XL 4007 laser systems worldwide due to a mechanical cooling issue that may cause the device to stop emitting laser pulses during surgery.

    Product
    AURIGA XL 4007 GENERAL SYSTEM UPN: M0068FS4007G0 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
  • HighFDA (Devices)·Z-1481-2019·2019-05-29

    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, 3x90mm, round shaft, Item Number ST502015630
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1397-2019·2019-05-29

    Boston Scientific Recalls Auriga 30 Laser Systems Due to Power Degradation

    Boston Scientific is recalling 18 Auriga 30 laser systems worldwide because a mechanical cooling issue may cause faster-than-normal power degradation and low power errors.

    Product
    AURIGA 30 GENERAL SYSTEM UPN: M0068S30G0 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 incision…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1446-2019·2019-05-29

    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, 3.5x90mm, round shaft, Item Number 502015635
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1310-2019·2019-05-29

    Integra LifeSciences Recalls MoniTorr CSF Drainage Systems Due to Stopcock Breakage

    Integra LifeSciences is recalling MoniTorr CSF Drainage Systems because the LimiTorr Transducer Mount and MoniTorr Panel Mount stopcocks may break.

    Product
    MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Valve MoniTorr 10102 10-102 CSF Drainage System w/Patient Line One Way Valve w MoniTorr 10110 10-110 CSF Drainage System used with Pole Mount System MoniTorr 10140 10-140 CSF Drainage System w/Vinyl Measuring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1415-2019·2019-05-29

    Stryker 15mm Drill Recalled for Potential Material Deviation

    Zimmer GmbH is recalling Stryker 15mm drills because an investigation found they may have been manufactured from a different material than specified.

    Product
    Drill, 15mm stop, 1x83mm, Stryker, Item Number 502015114
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1472-2019·2019-05-29

    Zimmer GmbH Recalls 3.5mm Orthopedic Drill Due to Material Concerns

    Zimmer GmbH is recalling specific 3.5mm orthopedic drills because they may have been manufactured from a different material than specified.

    Product
    Drill for 3.5mm screw, 2.5x120mm, AO, Item Number ST502015216
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1480-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Concerns

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

    Product
    Drill, cannulated, 2.8x120mm, AO, Item Number ST502015628
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1471-2019·2019-05-29

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

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

    Product
    Drill for 2.7mm screw, 2x120mm, AO, Item Number ST502015212
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1425-2019·2019-05-29

    Zimmer GmbH Recalls 26mm Orthopedic Drill Due to Material Concerns

    Zimmer GmbH is recalling specific orthopedic drills because they may have been manufactured from a different material than specified.

    Product
    Drill, 26mm stop, 1.4x81mm, AO, Item Number 502015146
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1393-2019·2019-05-29

    Boston Scientific Recalls Auriga XL 4007 Laser Systems Due to Power Degradation

    Boston Scientific is recalling three Auriga XL 4007 laser systems because a mechanical cooling issue may cause faster-than-normal power degradation and low power errors.

    Product
    AURIGA XL 4007 GENERAL - DEMO SYSTEM UPN: M0068FS4007GD0 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
  • HighFDA (Devices)·Z-1457-2019·2019-05-29

    Zimmer CBS 4.5 Countersink Recalled for Potential Material Deviation

    Zimmer GmbH is recalling CBS 4.5 countersinks because they may have been manufactured from a different material than specified.

    Product
    CBS 4.5 countersink, cannulated, 18mm stop, round-shaft, Item Number 503004351
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1384-2019·2019-05-29

    Beckman Coulter UniCel DxH 900 Hematology Analyzer Recall for Platelet Errors

    Beckman Coulter is recalling 341 UniCel DxH 900 hematology analyzers because they may produce erroneously elevated platelet results without warning, potentially masking low platelet counts.

    Product
    UniCel DxH 900 Coulter Cellular Analysis System, REF number C11478 Product Usage: Note: The DxH 900 hematology analyzer is CLIA categorized under document CR180294 and is currently marketed as a member of the instrument family of the DxH 800 cleared under K140911, per FDA s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1423-2019·2019-05-29

    Zimmer GmbH Recalls 2.5x135mm AO Drills Due to Material Concerns

    Zimmer GmbH is recalling 2.5x135mm AO Drills because they may be made from a different material than specified. The products were distributed to 41 US states.

    Product
    Drill, 2.5x135mm, AO, Item Number 502015142
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1413-2019·2019-05-29

    Zimmer GmbH Recalls Drill System Due to Potential Material Deviation

    Zimmer GmbH is recalling Drill Sys 2.7 units because they may have been manufactured from a material different from specifications.

    Product
    Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1427-2019·2019-05-29

    Zimmer GmbH Recalls 2.7mm Orthopedic Drills Due to Material Concerns

    Zimmer GmbH is recalling specific 2.7mm orthopedic drills because an investigation found they may be made from a different material than specified.

    Product
    Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1420-2019·2019-05-29

    Zimmer GmbH Recalls 19mm Orthopedic Drills Due to Material Concerns

    Zimmer GmbH is recalling specific 19mm orthopedic drills because they may be made from the wrong material. The devices were distributed to 38 US states.

    Product
    Drill, 19mm stop, 1.9x87mm, AO, Item Number 502015131
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1459-2019·2019-05-29

    Zimmer GmbH Recalls CBS 4.0 Countersink Due to Material Concerns

    Zimmer GmbH is recalling CBS 4.0 countersinks because they may have been manufactured from a different material than specified.

    Product
    CBS 4.0 countersink, cannulated, 30mm stop, AO, Item Number 503004353
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1473-2019·2019-05-29

    Zimmer GmbH Recalls 2.7mm AO Drills Due to Material Concerns

    Zimmer GmbH is recalling 2.7x125mm AO drills because they may be made from the wrong material. The devices were distributed to 40 US states.

    Product
    Drill, 2.7x125mm, AO , Item Number ST502015217
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1424-2019·2019-05-29

    Zimmer GmbH Recalls Stryker 26mm Drill Due to Material Concerns

    Zimmer GmbH is recalling Stryker 26mm drills because they may be made from the wrong material. The products were distributed to 39 US states.

    Product
    Drill, 26mm stop, 1.4x94mm, stryker, Item Number 502015145
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1439-2019·2019-05-29

    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, 2.5x95mm, AO, Item Number 502015621
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1368-2019·2019-05-29

    Roche Cobas infinity Software Recall for Missing Quality Control Alarms

    Roche Diagnostics is recalling 15 units of Cobas infinity software versions 2.0 through 2.5 because quality control alarms may fail to display after a bottle change.

    Product
    Cobas¿ infinity central lab IT solution Material Number: 07154003001 Calculator/Data Processing Module, For Clinical Use
    Category
    Medical Device
    Distribution
    11 states