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

19126–19150 of 27647

  • HighFDA (Devices)·Z-3221-2017·2017-10-04

    Teleflex Percuvance Johans Grasper Tool Tip Recall for Connection and Jaw Issues

    Teleflex Medical is recalling Percuvance Johans Grasper Tool Tips because the shaft connection may be compromised or the jaws may close abruptly.

    Product
    Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to…
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-3200-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 453 nonsterile orthopedic drill bits because raw material anomalies may cause instrument fracture during use.

    Product
    Drill Bit Quick-Connect Calibrated 3-Fluted 2.5 mm Diameter 230 mm Length, Item Number/EDI 00480723025, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3220-2017·2017-10-04

    Teleflex Recalls Percuvance Clip Applier Tool Tips Due to Connection Issues

    Teleflex Medical is recalling 20,039 Percuvance Clip Applier Tool Tips because the shaft connection may be compromised or the jaws may close abruptly.

    Product
    Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to…
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-3156-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fracture Fixation Long Drills

    Zimmer Biomet is recalling 10 units of ECT Internal Fracture Fixation Long Drills due to raw material anomalies that may increase the risk of instrument fracture.

    Product
    ECT Internal Fracture Fixation Long Drill, 6.4 mm (1/4 Inch) Diameter 20.3 cm(8 Inch) Length, Item Number/EDI 00129100406, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3170-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fracture Fixation Drill Bits

    Zimmer Biomet is recalling 1,255 ECT Internal Fracture Fixation Drill Bits due to raw material anomalies that may increase the risk of instrument fracture during use.

    Product
    ECT Internal Fracture Fixation Drill 3.2 mm Diameter (.126 Inch), Item Number/EDI 00231803200, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3147-2017·2017-10-04

    Zimmer Biomet Recalls M/DN Intramedullary Fixation Femoral Drill Bits

    Zimmer Biomet is recalling 25 units of M/DN Intramedullary Fixation Femoral Drills due to raw material anomalies that may increase the risk of instrument fracture during use.

    Product
    M/DN Intramedullary Fixation Femoral Drill 3.7 mm Diameter Replaces 2255-08-32, Item Number/EDI 00225503137, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3194-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Drill Bit Quick-Connect 2.7 mm Diameter 100 mm Length, Item Number/EDI 00480610027, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3179-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Surgical Instruments Due to Material Anomaly

    Zimmer Biomet is recalling 173 orthopedic surgical instruments because a material anomaly may increase the risk of instrument fracture during use.

    Product
    Zimmer Periarticular Locking Plate System Cannulated Drill Standard Quick-Connect 2.7 mm O.D., Item Number/EDI 00236017127, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3192-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 705 nonsterile orthopedic drill bits and screw taps because raw material anomalies may cause instrument fracture during use.

    Product
    Drill Bit Quick-Connect 1.5 mm Diameter 85 mm Length, Item Number/EDI 00480608515, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3153-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 25 nonsterile orthopedic drill bits because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Drill Bit Quick-Connect 1.1 mm Diameter 60 mm Length, Item Number/EDI 00480606011, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3182-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 418 ECT Internal Fracture Fixation Quick-Connect Drills because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    ECT Internal Fracture Fixation Quick-Connect Drill 2.0 mm Diameter 10 cm Length, Item Number/EDI 00241002000, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3154-2017·2017-10-04

    Zimmer Biomet Recalls NCB Periprosthetic Plate System Drill Bits

    Zimmer Biomet is recalling 300 nonsterile NCB Periprosthetic Plate System Drill Bits due to raw material anomalies that may increase the risk of instrument fracture during use.

    Product
    NCB Periprosthetic Plate System Drill Bit With Quick-Coupling 3.5 mm Diameter 195 mm Length, Item Number/EDI 0200024325, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3229-2017·2017-10-04

    Sorin Platinium ICDs Recalled for Potential Overconsumption Risk

    Sorin Group Italia SRL is recalling Platinium DR 1510 ICDs due to a possibility of overconsumption following ElectroStatic Discharge (ESD) during implant surgery or MRI scans.

    Product
    Platinium DR 1510, Model Number TDF032U, UDI/GTIN 08031527015521, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients who…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3195-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling specific nonsterile orthopedic drill bits because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    Drill Bit Quick-Connect 2.5 mm Diameter 110 mm Length, Item Number/EDI 00480611025, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3165-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fracture Fixation Drill Bits

    Zimmer Biomet is recalling 3,640 ECT Internal Fracture Fixation Drill Bits because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    ECT Internal Fracture Fixation Drill Bits 2.0 mm Diameter (.079 Inch) , Item Number/EDI 00231802006, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3145-2017·2017-10-04

    Zimmer Biomet Recalls Herbert Cannulated Bone Screw System Drills

    Zimmer Biomet is recalling 18 units of Herbert Cannulated Bone Screw System drills due to raw material anomalies that may increase the risk of instrument fracture.

    Product
    Herbert Cannulated Bone Screw System, Cannulated Main Drill 3.1 mm Diameter, Item Number/EDI 00115501500, Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3159-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Pilot Tips Due to Fracture Risk

    Zimmer Biomet is recalling 27 nonsterile orthopedic drill pilot tips because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    M/DN, Intramedullary Fixation Distal Drill Pilot Tip 3.7 mm Diameter Item Number/EDI 00225503337, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3168-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fracture Fixation Drills Due to Material Anomaly

    Zimmer Biomet is recalling 1,250 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.

    Product
    ECT Internal Fracture Fixation Drill 2.7 mm Diameter (.106 Inch), Item Number/EDI 00231802700, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3169-2017·2017-10-04

    Zimmer Biomet Recalls ECT Internal Fracture Fixation Drill Bits

    Zimmer Biomet is recalling 1,286 ECT Internal Fracture Fixation Drill Bits due to raw material anomalies that may increase the risk of instrument fracture during use.

    Product
    ECT Internal Fracture Fixation Drill Bits 2.7 mm Diameter (.106 Inch), Item Number/EDI 00231802706, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3222-2017·2017-10-04

    Teleflex Percuvance Maryland Dissector Tool Tip Recall for Connection Issues

    Teleflex Medical is recalling Percuvance Maryland Dissector Tool Tips because the shaft connection may be compromised or the jaws may close abruptly.

    Product
    Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips…
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-3236-2017·2017-10-04

    Novadaq SPY-PHI Drape Recall Due to Potential Sterile Barrier Breach

    Novadaq is recalling SPY-PHI Drapes because pinholes may compromise the sterile barrier. The product is used to cover surgical equipment, not patients.

    Product
    NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes), Sterile, Rx.. Manufactured for: Novadaq Technologies Inc., Burnaby, BC, Canada. The SPY-PHI Drape is intended to cover the SPY-PHI System to maintain a sterile field, and as an aid in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3190-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk

    Zimmer Biomet is recalling 30 units of orthopedic drill bits because raw material anomalies may cause the instruments to fracture during use.

    Product
    Drill Bit Jacobs Chuck 2.0 mm Diameter 85 mm Length, Item Number/EDI 00480508520, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3144-2017·2017-10-04

    Zimmer Biomet Recalls Sterile Shoulder System Drills Due to Fracture Risk

    Zimmer Biomet is recalling 2,825 sterile shoulder system drills manufactured with raw material anomalies that may increase the risk of instrument fracture.

    Product
    Zimmer Trabecular Metal Reverse Shoulder System Instrumentation, Drill 2.5 mm Diameter, Item Number/EDI 47430904601, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3234-2017·2017-10-04

    Novadaq SPY-PHI Drape Recalled for Potential Sterile Barrier Breach

    Novadaq is recalling SPY-PHI Drapes because pinholes may compromise the sterile barrier. The product is intended for equipment coverage, not patient contact.

    Product
    NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH2000 (single drape), Sterile, Rx. Manufactured for: Novadaq Technologies Inc., Burnaby, BC, Canada. The SPY-PHI Drape is intended to cover the SPY-PHI System to maintain a sterile field, and as an aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3201-2017·2017-10-04

    Zimmer Biomet Recalls Orthopedic Surgical Drills Due to Fracture Risk

    Zimmer Biomet is recalling specific orthopedic surgical drills and screw taps because raw material anomalies may cause the instruments to fracture during use.

    Product
    Zimmer Natural Nail System Freehand Drill 4.3 mm Diameter 152.5 mm Length, Item Number/EDI 00249007543, Nonsterile. orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide