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

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

33251–33275 of 40449

  • ModerateFDA (Devices)·Z-1508-2015·2015-04-29

    Specialty Appliance Works Recalls Universal Nuts for Herbst Appliances

    Specialty Appliance Works is recalling Universal Nuts used in Herbst orthodontic appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    LR Telescoping Cantilever Arms (5/pk) and LL Telescoping Cantilever Arms (5/pk) A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1481-2015·2015-04-29

    Catheter Research Recalls Mislabeled HSG Trays and Catheters

    Catheter Research, Inc. is recalling 880 HSG trays and catheters because the flexible and shapeable catheters were mislabeled on the packaging.

    Product
    HSG Trays/HS 5F Catheter Combo; HSG Procedure Tray+ Shapeable 5F HSG catheter. For hysterosonography and hysterosalpingography, gynecological use.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1506-2015·2015-04-29

    Specialty Appliance Works Recalls Universal Nuts for Incorrect Material Composition

    Specialty Appliance Works is recalling Universal Nuts used in orthodontic Herbst Appliances because they were manufactured with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 mm A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1465-2015·2015-04-29

    Biomet Recalls Lineum HF Torque Handle Limit Due to Component Updates

    Biomet Spine is recalling 148 Lineum HF Torque Handle Limit units because the supplier withdrew the product for component updates or reconfiguration.

    Product
    Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct Usage: Designed to facilitate reconstruction of the cervical and upper thoracic spine using bones screws, locking plugs, and various types of rods, hooks, and lateral connectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1507-2015·2015-04-29

    Specialty Appliance Works Recalls Universal Nuts for Orthodontic Appliances

    Specialty Appliance Works is recalling Universal Nuts for orthodontic Herbst Appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    HTM Mechanism Set Set 16, HTH Mechanism Set Size 18, HTH Mechanism Set Size 21 and HTH Mechanism Set Size 24 A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1479-2015·2015-04-29

    SpineFrontier Recalls MISquito Pedicle Screw System Surgical Technique Document

    SpineFrontier is recalling the MISquito Pedicle Screw System Surgical Technique document because it does not adequately convey the intended use of the Rod Caliper.

    Product
    SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique; Part Number: DOC80023. The Rod Caliper is a manual surgical instrument that may be used as part of the PedFuse Pedicle Screw System and its MISquito components during percutaneous, minimally…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1449-2015·2015-04-22

    Hansen Medical Recalls Magellan Robotic Systems Due to Catheter Retraction Defect

    Hansen Medical is recalling 19 Magellan Robotic Systems because the catheter may fail to stop retracting when the control button is released.

    Product
    Magellan Robotic System; Model No(s). 11132 and 11139. A steerable catheter control system used at clinical sites.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1441-2015·2015-04-22

    GE Healthcare Recalls Improperly Installed Ceiling Suspended Radiation Shields

    GE Healthcare is recalling 797 ceiling-suspended pendent systems for radiation shields and surgical lamps due to improper installation. One incident of a shield falling and causing a minor injury has been reported.

    Product
    Kenex Radiation Shield installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1451-2015·2015-04-22

    Baxter SIGMA Spectrum Infusion Pump Software Recall for Dose Display Discrepancy

    Baxter is recalling SIGMA Spectrum Infusion Pump software due to a discrepancy between Master Drug Library settings and pump display, which may cause therapy delays or unintended delivery rates.

    Product
    Master Drug Library Software version 8.0, Product Code 35723V080, to be used with SIGMA Spectrum Infusion System (Pump) version 8.0, Product Code 35700BAX2 The SIGMA Spectrum Infusion Pump with Master Drug Library (MDL) is intended to be used for the controlled…
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-1442-2015·2015-04-22

    Baylis Medical Recalls ProTrack Microcatheter Due to Circumferential Shaft Defects

    Baylis Medical Corp is recalling two lots of ProTrack Microcatheters due to potential circumferential defects along the device shaft.

    Product
    ProTrack Microcatheter; Product Usage: The ProTrack Microcatheter is a sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1443-2015·2015-04-22

    Bard PICC and Dialysis Catheter Kits Recalled for Scalpel Injury Risk

    Bard Access Systems is recalling PICC and dialysis catheter kits containing Safe-Cut Safety Scalpels due to the potential for inadvertent scalpel stick injuries.

    Product
    Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter kits containing Safe-Cut Safety Scalpels.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1453-2015·2015-04-22

    US Endoscopy Recalls Talon Grasping Devices Due to Detached Wire Component

    US Endoscopy Group Inc is recalling 1,695 Talon Grasping Devices because a wire component on the distal grasping assembly became detached.

    Product
    Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1447-2015·2015-04-22

    Bard Monopty Disposable Core Biopsy Instruments Recalled for Activation Issues

    Bard Peripheral Vascular is recalling specific Bard Monopty Disposable Core Biopsy Instruments and Kits due to potential activation-related issues.

    Product
    Bard Monopty Disposable Core Biopsy Instruments and Kits, Monopty 14g x 16cm (22mm), Product Code: 121416; Monopty Biopsy, Product Code: 000441; Monopty 14g x 10cm (22mm), Product Code: 121410; Monopty 14g x 10cm (11mm), Product Code: 211410. The BARD MONOPTY Disposable Core…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2015·2015-04-22

    CooperSurgical Recalls Wallach LL 100 Cryosurgical Units Due to Gas Line Burst Risk

    CooperSurgical is recalling 255 Wallach LL 100 cryosurgical units because an internal gas line may malfunction and burst under pressure.

    Product
    WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number 900019-70; LL100 Multi Tip W/TC - Part Number: 900629; LL100 - CO2 - Part Number 900162
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2015·2015-04-22

    Bard ConQuest PTA Balloon Dilatation Catheter Recalled for Deflation Risk

    Bard Peripheral Vascular is recalling specific lots of the ConQuest PTA Balloon Dilatation Catheter due to a risk of deflation-related issues.

    Product
    Bard ConQuest PTA Balloon Dilatation Catheter, 12mm Balloon Size, Product Code: CQ-75124.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1444-2015·2015-04-22

    Hardy Diagnostics Recalls HardyCHROM SS Agar Due to Color Development Issue

    Hardy Diagnostics is recalling HardyCHROM SS Agar (Lot 15037) due to a report of possible lack of color development in Shigella organisms.

    Product
    Hardy Diagnostics cat no. G327 HardyCHROM SS Agar (HardyCHROM Salmonella Shigella) Cat no: G327 Container type: 15x100mm monoplate Packaged: 10 plates/sleeve Storage: 2 to 8 degrees C. on receipt in dark A selective chromogenic medium for the primary screening…
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1435-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Issue

    Nobel Biocare is recalling 216 units of NobelReplace CC PMC NP dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NobelReplace CC PMC NP 3.5x11.5mm, Article No. 37287.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1416-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 24 units of Replace Select Tapered TiU NP 3.5x16mm dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    Replace Select Tapered TiU NP 3.5x16mm, Article No. 29403. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1432-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Issue

    Nobel Biocare is recalling 56 dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NobelReplace CC RP 5.0x8mm, Article No. 36710.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1452-2015·2015-04-22

    Integra Flowable Wound Matrix Recalled for Stability Criteria Failures

    Integra LifeSciences is recalling 287 packages of Flowable Wound Matrix because the product failed stability acceptance criteria for visual appearance and force vs. displacement.

    Product
    Integra¿ Flowable Wound Matrix Size 3cc 1 unit/box single use, sterile device Rx Only Model Number FWD301 (US) & FDR301 (Non-US) Flowable Wound Matrix is comprised of the following components which are provided in a sealed and sterilized Tyvek / plastic tray: - An empty…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1439-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 53 units of NobelReplace CC PMC RP 5.0x10mm dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NobelReplace CC PMC RP 5.0x10mm, Article No. 37296.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1446-2015·2015-04-22

    Biomet Recalls Low Profile Non-Locking Screws Due to Anodizing Error

    Biomet is recalling 45 Low Profile Non-Locking Screws because they were anodized green instead of the required gold color.

    Product
    LOW PROFILE NON-LOCK SCREW; 2.7mm x 22 mm; REF 131227222; LOT RM105E. Provides the orthopaedic surgeon a means of bone fixation and helps generally in the management of fractures and reconstructive surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1420-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Contamination

    Nobel Biocare is recalling 74 dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NOBELREPLACE Tapered Groovy RP 4.3x10mm, Article No. 32216. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1421-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 7 dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NOBELREPLACE Tapered Groovy 6.0 6x8mm, Article No. 32223. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1414-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 131 units of Replace Select Tapered TiU NP dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    Replace Select Tapered TiU NP 3.5x10mm, Article No. 29401. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide