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

Agency

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

32551–32575 of 40325

  • ModerateFDA (Devices)·Z-2068-2015·2015-07-22

    Nidek GYC-1000 Laser Accessories Recalled for Missing Labels

    Nidek Inc is recalling GYC-1000 laser accessories because they are missing Laser Aperture labels. The affected units were distributed to 13 US states.

    Product
    Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator System; GYC4EP-01 0W02 and GYC4EP-1 0Z20; The Nidek Green Laser Photocoagulator Model GYC- 1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation…
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-2086-2015·2015-07-22

    Synthes Recalls 16mm Chisel Blades Due to Incorrect Size Marking

    Synthes (USA) Products LLC is recalling 100 units of 16mm Chisel Blades that were incorrectly etched as 16mm when they are actually 10mm.

    Product
    16mm Chisel Blade; used in the LCP Anterior Ankle Arthodesis Plate System and the Hip Preservation Surgery Set. Orthopedic manual surgical instrument.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2071-2015·2015-07-22

    Exactech Single Barrel Drill Guides Recalled for Incomplete Final Inspection

    Exactech, Inc. is recalling two Single Barrel Drill Guides shipped to a single consignee in Florida before final inspection was completed.

    Product
    Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2075-2015·2015-07-22

    Musculoskeletal Transplant Foundation Recalls Allofix Insertion Kits Due to Drill Size Labeling Error

    Musculoskeletal Transplant Foundation is recalling 117 Allofix Insertion Kits because they are labeled as 2.0mm but may contain 2.4mm drills.

    Product
    Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orthopedic surgeon and are intended to be used in conjunction with the associated allograft. This kit is for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2074-2015·2015-07-22

    Nobel Biocare Recalls Zirconia Abutment Retrieval Instruments Due to Dimensional Error

    Nobel Biocare is recalling 149 units of Zirconia Abutment Retrieval Instruments and Kits because a dimensional error prevents the instruments from removing metal adapters as intended.

    Product
    Abutment Retrieval Instrument Zirconia CC RP/WP, Article No. 37882 and Abutment Retrieval Kit, Article No. 37508 (Article No. 37882 was assembled in this kit). Used to remove a zirconia abutment if the abutment is stuck in the implant connection due to a tight seat. Endosseous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2087-2015·2015-07-22

    Eizo RadiForce GX540 Monitors Recalled for Display Abnormalities

    Eizo is recalling 19 RadiForce GX540 monitors that may display abnormally when connected to specific graphics boards with DisplayPort.

    Product
    RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2091-2015·2015-07-22

    Synthes Recalls Helical Blade Inserter for TFNA Due to Sizing Defect

    Synthes (USA) Products LLC is recalling 32 units of the Helical Blade Inserter for TFNA because an oversized pin prevents the tool from passing through the guide sleeve.

    Product
    Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA); intended to secure the head element to the head element inserter to prevent disengagement during head element insertion. Manual orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2066-2015·2015-07-22

    Tosoh Glycohemoglobin Analyzer Buffer Recalled for Incorrect Expiration Date Labeling

    Tosoh Bioscience is recalling G7 Variant Elution Buffer HiS no. 1 (M) because it is labeled with an expiration date of October 2015 instead of the correct October 2014.

    Product
    G7 Variant Elution Buffer HiS no. 1 (M) component of the Tosoh Automated Glycohemoglobin Analyzer HLC 723G7. Product Usage: G7 Variant Elution Buffer HiS No 1. (M) is one of the buffers used on Tosoh Automated Glycohemoglobin Analyzer HLC 723G7.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2090-2015·2015-07-22

    BD Biosciences Recalls Flow Cytometers for Missing Laser Safety Labeling

    BD Biosciences is recalling 2,188 flow cytometers installed between June 2007 and September 2011 because they lack required FDA laser safety labeling.

    Product
    BD Flow Cytometers; used on all BD FACSCount, BD FACSCalibur, BD FACSCanto, BD FACSCanto II, BD LSR II, BD LSRFortessa,BD FACSAria, BD FACSAria II, BD FACSAria Ill, BD lnflux, BD FACSArray,BD Pathway 855, BD Pathway 435 and all SORP instruments. BD Biosciences Flow cytometers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1951-2015·2015-07-15

    Shiley Pediatric Tracheostomy Tubes Recalled for Breathing Difficulties

    FDA recalls Shiley tracheostomy tubes due to reports of patient discomfort and breathing difficulties.

    Product
    Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube with TaperGuard Cuff. Intended for use in providing tracheal access for airway managements.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1989-2015·2015-07-15

    Alliance Partners Recalls Nakoma-SL Cervical Plating Drill Guides

    Alliance Partners LLC is recalling 21 Nakoma-SL Anterior Cervical Plating System drill guides because screws may advance through the plate during implantation.

    Product
    Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System is intended for anterior intervertebral screw fixation of the cervical spine at levels C2-T1. The Nakoma ACP System is indicated for temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2046-2015·2015-07-15

    Biomet Recalls A.L.P.S. Foot Locking Calcaneus Plates Due to Thread Defects

    Biomet is recalling 75 A.L.P.S. Foot Locking Calcaneus Plates because thread defects may cause screws to back out or shear, potentially requiring revision surgery.

    Product
    A.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a means of bone fixation and helps generally in the management of fractures and reconstructive surgeries.
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1950-2015·2015-07-15

    Shiley Neonatal and Pediatric Tracheostomy Tubes Recalled for Breathing Difficulties

    FDA is recalling Shiley Neonatal and Pediatric Tracheostomy Tubes because patients reported discomfort and breathing difficulties after switching to these products.

    Product
    Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube, Cuffless. Model Numbers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2015·2015-07-15

    Maquet Surgical Light Suspension Arms Recalled for Debris Risk

    Maquet is recalling 646 PowerLED, X-TEN, and VOLISTA surgical light systems because suspension arms may grind and release paint chips into the surgical field.

    Product
    The PowerLED / X-TEN / VOLISTA Surgical Light Systems are surgical light systems intended to be used to provide visible illumination of the surgical area or the patient. Ceiling surgical light systems typically include one or more arms that are able to rotate 360 degrees around…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1987-2015·2015-07-15

    Philips GoSafe Communicator 7000L Personal Emergency Response System Recall

    Lifeline Systems is recalling 38 Philips GoSafe Communicator 7000L units because they may fail to sense the phone line under unusual landline conditions.

    Product
    Philips GoSafe Communicator 7000L Personal emergency response system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2015·2015-07-15

    BTE Technologies Recalls Primus Exercise Devices Due to Detachment Risk

    BTE Technologies is recalling 510 Primus rehabilitation devices because the optional Chop / Lift Bar may detach, posing a fall hazard to users.

    Product
    Primus (THE BTE WS30), model PrimusRS (PRRS) and Primus+ (PR30) a measuring exercise equipment device designed to provide active and passive torque resistance to patient motion during rehabilitation therapy. The Primus that includes the optional Chop / Lift Bar.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2034-2015·2015-07-15

    Stradis Pediatric Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Pediatric Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.

    Product
    Pediatric Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1993-2015·2015-07-15

    Stradis Basic Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Basic Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.

    Product
    Basic Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2015·2015-07-15

    Stradis Arthroscopy Packs Recalled Due to Component Recall

    Stradis Healthcare is recalling Arthroscopy Packs because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.

    Product
    Arthroscopy Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2045-2015·2015-07-15

    Volcano ComboMap Intravascular System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 ComboMap Intravascular Flow and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia Physiomonitoring System.

    Product
    ComboMap Intravascular Flow and Pressure System; Product/Part number: Combo Map - 802745-001. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and vascular structures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2023-2015·2015-07-15

    Stradis Healthcare Recalls Eye Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Eye Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.

    Product
    Eye Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2021-2015·2015-07-15

    Stradis Gyn Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Gyn Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.

    Product
    Gyn Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide