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.

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32376–32400 of 40325

  • ModerateFDA (Devices)·Z-2234-2015·2015-08-05

    EXP Pharmaceutical Services Recalls Unregistered Transcatheter Septal Occluders

    EXP Pharmaceutical Services Corp is recalling 12mm vascular transcatheter septal occluders because the company failed to register as a medical device establishment or establish a quality system.

    Product
    Medical Device Exchange 12MM VASCULAR; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 9-AVP2-012; EXP (repackager), Aga Medical (OEM) Transcatheter septal occluder
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2287-2015·2015-08-05

    Anspach Fluted Barrel Dissection Tools Recalled for Labeling Inconsistency

    The Anspach Effort, Inc. is recalling 110 fluted barrel dissection tools because the labeled shaft exposure may be inconsistent with actual usage.

    Product
    ANSPACH - Fluted Barrel; 8MM x 12.5MM REF L-8BA-G1 Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2265-2015·2015-08-05

    Ivoclar Vivadent Recalls IPS Empress Universal Glaze Spray Due to Coarse Particles

    Ivoclar Vivadent is recalling IPS Empress Universal Glaze Spray because complaints indicated coarse particles in the glazed surface of dental restorations.

    Product
    IPS Empress Universal Glaze Spray 270 mL, Product Code/Model/Catalog Number 609432AN, Rx only. Porcelain glaze spray used in the fabrication of dental restorations
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-2219-2015·2015-08-05

    EXP Pharmaceutical Services Recalls Unregistered Implantable Staple Loading Units

    EXP Pharmaceutical Services Corp is recalling three units of implantable staple loading units because the company failed to register as a medical device establishment or maintain a quality system.

    Product
    Medical Device Exchange - Loading Unit w/ DST Series Technology 60mm - 3.5mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number TA6035L; EXP (repackager), Covidien (OEM) Implantable Staple
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2263-2015·2015-08-05

    McKesson Paragon Laboratory Management Software Recall for Data Display Errors

    McKesson Technologies is recalling Paragon Laboratory Management software versions 12.1 and 12.1.1 because the Final Cumulative Report may display incorrect data when used with Microsoft SQL Server 2012.

    Product
    Paragon Laboratory Management
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2303-2015·2015-08-05

    Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling

    The Anspach Effort, Inc. is recalling 118 G1 dissection tools because the specified shaft exposure on the label may not be consistent with all listed attachments.

    Product
    ANSPACH - 5MM Fluted Ball, Extends 27MM; REF M-5B-27-G1. Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2210-2015·2015-08-05

    MTF Recalls Allograft Cortical Pins Due to Diameter Labeling Error

    Musculoskeletal Transplant Foundation is recalling one lot of Allograft Cortical Pins because the 2.0 mm label may contain 2.4 mm pins.

    Product
    Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2223-2015·2015-08-05

    EXP Pharmaceutical Services Recalls Unregistered Medical Suction Devices

    EXP Pharmaceutical Services Corp is recalling sterile suction devices because the company failed to register as a medical device establishment or maintain its own quality system.

    Product
    Medical Device Exchange - Silicone Round Drain; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number SU130-1321; EXP (repackager), Jackson Pratt (OEM) Apparatus, suction, single patient use, portable, nonpowered
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2296-2015·2015-08-05

    Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling

    The Anspach Effort, Inc. is recalling 103 G1 dissection tools because the specified shaft exposure may be greater than labeled when used with certain attachments.

    Product
    ANSPACH - 5MM x 11.3MM Fluted Barrel; REF M-5BA-A-G1 Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2239-2015·2015-08-05

    EXP Recalls Unregistered Medical Device Exchange Round Diamond Bur

    EXP Pharmaceutical Services Corp is recalling Round Diamond Bur Extra Coarse devices because the company failed to register as a medical device establishment or maintain a quality system.

    Product
    Medical Device Exchange Round Diamond Bur Extra Coarse; 3.0mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 5820-10-130; EXP (repackager), Stryker (OEM) Drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2227-2015·2015-08-05

    EXP Pharmaceutical Services Recalls Unregistered Implantable Skin Staple Systems

    EXP Pharmaceutical Services Corp is recalling three units of implantable skin staple systems because the company failed to register as a medical device establishment or establish a quality system.

    Product
    Medical Device Exchange -SYSTEM, TACKER SKIN 5MM; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 6206; EXP (repackager), Covidien (OEM) Implantable Staple
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2248-2015·2015-08-05

    EXP Pharmaceutical Services Recalls Unregistered Medical Device Repackaging Operations

    EXP Pharmaceutical Services Corp is recalling 12x40 Airway Stent Systems due to failure to register as a medical device establishment and lack of a quality system.

    Product
    Medical Device Exchange 12x40 Airway Stent System; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 90129-212; EXP (repackager), Aero (OEM) Prosthesis, tracheal, expandable
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2306-2015·2015-08-05

    Anspach Effort Recalls G1 Dissection Tools Due to Labeling Inconsistencies

    The Anspach Effort, Inc. is recalling 796 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure than specified.

    Product
    ANSPACH -4MM Carbide Fluted Ball, Extends 27MM; REF S-4BL-C-G1. Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2282-2015·2015-08-05

    Anspach Extra Coarse Diamond Drum Recalled for Inconsistent Shaft Exposure

    The Anspach Effort, Inc. is recalling 88 Extra Coarse Diamond Drums because the shaft exposure may be greater than labeled when used with certain attachments.

    Product
    ANSPACH - Extra Coarse Diamond Drum, 6.8MM x 10.6MM REF L-68DRMDX-G1 Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2214-2015·2015-08-05

    EXP Recalls 5.5mm BioComposite Corkscrew Suture Anchor Due to Registration Failure

    EXP Pharmaceutical Services Corp is recalling 5.5mm BioComposite Corkscrew Suture Anchors because the company failed to register as a medical device establishment or maintain its own quality system.

    Product
    Medical Device Exchange - 5.5mm BioComposite Corkscrew FT, Vented Suture Anchor; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number AR-1927BCF; EXP (repackager), Arthrex (OEM) Fastener, fixation, nondegradable, soft tissue
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2222-2015·2015-08-05

    EXP Pharmaceutical Services Recalls Mayfield Disposable Skull Pins

    EXP Pharmaceutical Services Corp is recalling Mayfield Disposable Skull Pins because the company failed to register as a medical device establishment or maintain its own quality system.

    Product
    Medical Device Exchange - Mayfield Disposable Skull Pin; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number A1072; EXP (repackager), Integra (OEM) Holder, head, neurosurgical (skull clamp)
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2266-2015·2015-08-05

    Philips Invivo Expression MRI Patient Monitoring System Labeling Recall

    Philips is recalling 697 MRI patient monitoring systems because the labeling inaccurately lists endotracheal as a valid body temperature application site for the FlexTEMP sensor.

    Product
    Invivo Expression MRI Patient Monitoring System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2285-2015·2015-08-05

    Anspach Fluted Drum Dissection Tools Recalled for Inconsistent Shaft Exposure

    The Anspach Effort, Inc. is recalling 115 fluted drum dissection tools because the specified shaft exposure may be inconsistent with certain attachments, potentially resulting in greater exposure than labeled.

    Product
    ANSPACH - Fluted Drum, Side Cut Only; 7MM x 14MM REF L-7DRC-G1 Cutting shaping bone including spine and cranium.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2232-2015·2015-08-05

    EXP Pharmaceutical Services Recalls Laparoscopic Insufflation Needles

    EXP Pharmaceutical Services Corp is recalling two units of laparoscopic insufflation needles due to regulatory non-compliance regarding establishment registration and quality systems.

    Product
    Medical Device Exchange Insufflation Needle; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number C2201; EXP (repackager), Medline (OEM) Insufflator, laparoscopic
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2212-2015·2015-08-05

    EXP Pharmaceutical Services Recalls GelPort Laparoscopic Systems for Registration Violations

    EXP Pharmaceutical Services Corp is recalling three GelPort Laparoscopic Systems because the company failed to register as a medical device establishment or maintain its own quality system.

    Product
    Medical Device Exchange - GelPort Laparoscopic System; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number C8XX2N0NCE. EXP (repackager), Applied Medical (OEM) Laparoscope, General & Plastic Surgery.
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2251-2015·2015-08-05

    EXP Recalls Chocolate Balloon Catheters Due to Registration Deficiencies

    EXP Pharmaceutical Services Corp is recalling one unit of a Chocolate Balloon Catheter because the company failed to register as a medical device establishment or maintain its own quality system.

    Product
    Medical Device Exchange Chocolate Balloon Catheter/Over-the-Wire; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number CF14-150-25040-OTW. EXP (repackager), TriReme Medical (OEM) Catheter, angioplasty, peripheral, transluminal
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2274-2015·2015-08-05

    Hardy Diagnostics Recalls Multiple Clinical Culture Media Due to Lack of Clearance

    Hardy Diagnostics is recalling several clinical culture media products, including BHI with Ciprofloxacin, because they lack FDA 510(k) clearance.

    Product
    Hardy Diagnostics BHI with CIPRO, 1ug/ml container type: 16x100mm tube packaged: 20 tubes/box Product Usage: Brain Heart Infusion Broth with Ciprofloxacin, 1ug is for use as pre-enrichment broth for the cultivation of ciprofloxacin-resistant organisms from clinical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2238-2015·2015-08-05

    EXP recalls Stryker Round Fluted Burs due to registration violations

    EXP Pharmaceutical Services Corp is recalling Stryker Round Fluted Burs because the company failed to register as a medical device establishment or maintain a quality system.

    Product
    Medical Device Exchange Round Fluted Bur Soft Touch; 2.0mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 5820-10-120; EXP (repackager), Stryker (OEM) Drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2226-2015·2015-08-05

    EXP Recalls Unregistered Implantable Clips Due to Regulatory Non-Compliance

    EXP Pharmaceutical Services Corp is recalling 17 units of implantable clips because the company failed to register as a medical device establishment or maintain a quality system.

    Product
    Medical Device Exchange -APPLIER, MULTICLIP ROTATING; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 3299; EXP (repackager), Covidien (OEM) Clip, implantable
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2229-2015·2015-08-05

    EXP Recalls ETS FLEX 45 Endoscopic Articulating Linear Cutters

    EXP Pharmaceutical Services Corp is recalling ETS FLEX 45 endoscopic cutters because the company failed to register as a medical device establishment or maintain its own quality system.

    Product
    Medical Device Exchange ETS FLEX 45 ENDOSCOPIC ARTICULATING LINEAR CUTTER, 45MM STAPLE; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number ATS45; EXP (repackager), Ethicon (OEM) Implantable Staple.
    Category
    Medical Device
    Distribution
    6 states