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 deaths or serious injuries are reported, 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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

5101–5125 of 27364

HighFDA (Devices)·Z-2183-2024·2024-07-03
Siemens AXIOM MULTIX MP X-ray Tables Recalled for Power Supply Fire Risk
Siemens Medical Solutions is recalling AXIOM MULTIX MP radiographic X-ray tables due to a potential short circuit in the power supply that may cause overheating and fire. The recall includes 20 units with U.S. nationwide distribution.
Product
AXIOM MULTIX MP - Inended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395431
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2217-2024·2024-07-03
NovaGuide 2 Ultrasound System Recall Due to Grounding Cable Disconnection Risk
NovaGuide 2 Traditional Ultrasound systems may have grounding cables that can be inadvertently disconnected during use, creating risk of electrical shock and equipment malfunction. Twenty-eight systems have been distributed nationwide.
Product
NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2180-2024·2024-07-03
X-ray Table Touch Display Power Supply Fire Hazard
Siemens is recalling AXIOM MULTIX MT X-ray patient tables due to a potential short circuit in the Touch Display power supply that may cause overheating and fire. Fifty units were distributed nationwide.
Product
AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395399
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2204-2024·2024-07-03
Medtronic Implantable Cardioverter Defibrillator Recalled Due to Weld Crack Defect
Medtronic is recalling 6 units of the MIRRO MRI VR SureScan implantable cardioverter defibrillator due to a potential manufacturing defect. The devices failed manufacturing quality checks because of a weld crack.
Product
MIRRO MRI VR SureScan, Model Number DVME3D1, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2169-2024·2024-07-03
GE CARESCAPE Canvas Smart Display monitors may fail to restart after power loss
GE CARESCAPE Canvas Smart Display monitors may fail to turn on after a power loss, particularly following battery replacement, potentially delaying recognition of patient condition changes.
Product
CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c) 5939590-102; monitor, physiological, patient
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2198-2024·2024-07-03
Medtronic EVERA MRI implantable defibrillator recalled for manufacturing weld defect
Medtronic is recalling five units of its EVERA MRI S DR SureScan implantable cardioverter defibrillator due to a manufacturing defect—a weld crack that caused failure during quality control testing.
Product
EVERA MRI S DR SureScan, Model Number DDMC3D1, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2199-2024·2024-07-03
Implantable Cardioverter Defibrillator with Weld Crack Defect Recalled
Medtronic is recalling 40 EVERA MRI S DR SureScan ICDs (Model DDMC3D4) due to manufacturing weld cracks that caused devices to fail leak tests. The defect was identified during manufacturing; no patient harm has been reported.
Product
EVERA MRI S DR SureScan, Model Number DDMC3D4, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2185-2024·2024-07-03
AXIOM Vertix Solitaire Medical Imaging Device Recall: Fire Risk from Power Supply Defect
Siemens is recalling 4 AXIOM Vertix Solitaire medical imaging devices due to a short circuit in the touch display power supply that may cause overheating and fire. Units with serial numbers 1004, 1006, 1011, and 1014 are affected.
Product
AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: 8627718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2186-2024·2024-07-03
Siemens Multix TOP X-ray Table Recalled Due to Fire Risk
Siemens is recalling 3 Multix TOP I PRO radiographic X-ray tables due to a short circuit in the Touch Display power supply unit that may cause overheating and fire.
Product
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2207-2024·2024-07-03
Medtronic COBALT DR MRI SureScan ICD Recalled Due to Manufacturing Weld Crack
Medtronic is recalling 36 COBALT DR MRI SureScan implantable cardioverter defibrillators due to a weld crack manufacturing defect. The defect was identified during manufacturing quality checks.
Product
COBALT DR MRI SureScan, Model Number DDPB3D4, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2187-2024·2024-07-03
X-ray table recalled for fire hazard from power supply unit short circuit
Siemens MULTIX TOP I PRO X-ray tables are recalled due to a power supply short circuit that may cause overheating and fire. Three units have been identified.
Product
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 475525
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2221-2024·2024-07-03
Endoscopic Kittner Surgical Instrument Recalled for Sterile Barrier Defect
ASPEN SURGICAL is recalling 1,900 units of the Endoscopic Kittner Blunt Dissecting Instrument (Model KT-9101) due to a potential defect in the sterile barrier seal.
Product
Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2176-2024·2024-07-03
VASOVIEW HemoPro harvesting system fluid ingress may disable cautery
Maquet Cardiovascular recalls VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems due to fluid ingress into the harvesting tool handle, which may prevent necessary cautery or cause unintended cautery during surgical procedures.
Product
The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2201-2024·2024-07-03
Medtronic MIRRO MRI implantable defibrillator recalled for weld defect
Medtronic is recalling 3 MIRRO MRI DR SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality checks. The defect was detected during manufacturing before devices reached patients.
Product
MIRRO MRI DR SureScan, Model Number DDME3D1, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2174-2024·2024-07-03
Blood Glucose Meter Recall: Accu-Chek Guide May Display Incorrect Measurement Units
Roche is recalling Accu-Chek Guide (SC) blood glucose meters that may display readings in mmol/L instead of mg/dL, appearing approximately 18 times lower than actual. This could lead to incorrect treatment decisions and long-term diabetes complications.
Product
Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. Product REF Number: 08453071001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2167-2024·2024-07-03
FDA Recalls CUSA Excel Surgical Handpiece for Housing Cracks
Integra LifeSciences is recalling CUSA Excel C2600 surgical handpieces due to potential housing cracks that may delay treatment. The recall affects 2,652 units distributed nationwide and internationally.
Product
CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard tissue Catalog Number: C2600* *Note: you may see C2600P or C2600SRL on labeling. This notice is applicable for those SKUs as w
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2130-2024·2024-06-26
Ventilator Operator's Guide Recalled for Missing Critical MRI Safety Information
ZOLL is recalling operator's guides for the ZOLL 731 Ventilator because they omit critical MRI safety information. Missing distance guidance could cause the ventilator to malfunction during MRI procedures.
Product
ZOLL 731 Ventilator (EMV+, AEV, Eagle II) - for MRI Compatible Devices - Operator's Guide and Quick Reference Guide (QRGs) as follows: Part Numbers: 1. 799-EGL2-02 2. 799-EGL2-02-01 3. 799-EGL2-02-04 4. 799-EGL2-02-05 5. 799-EGL2-02-08 6. 799-EGL2-02-10 7. 799-EGL2-02-
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2020-2024·2024-06-26
Ventilator HAMILTON-C6 may fail to restart, risking oxygen deprivation
Hamilton Medical AG is recalling the HAMILTON-C6 ventilator due to a sensor failure that may prevent re-initiation after reconnection, potentially causing hypoxia.
Product
Ventilator HAMILTON-C6, PN: 160021
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2152-2024·2024-06-26
Storage Case Design Flaw May Allow Reuse of Single-Use Surgical Instruments
Howmedica Osteonics Corp. is recalling HRIS Storage & Sterilization Cases (Part 6210-9-900) due to a design flaw that may allow reuse and resterilization of single-use, sterile instruments. This poses a contamination and infection risk.
Product
HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2153-2024·2024-06-26
Howmedica Gray Revision Instrument Tray Recalled for Design Enabling Instrument Reuse
Howmedica is recalling the Gray Revision Instrument System Accessory Tray/Case due to a design flaw that may enable reuse and re-sterilization of single-use, sterile-packaged instruments.
Product
Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2158-2024·2024-06-26
Exactech OPTETRAK Knee Implants Recalled for Out-of-Specification Vacuum Bag Packaging
Exactech is recalling OPTETRAK Advanced Patella knee implant components packaged in vacuum bags that did not meet manufacturing specifications. Improper packaging could compromise product sterility.
Product
OPTETRAK, Advanced Patella, 3 Peg Implant, Item Numbers: a) 200-07-26, 26MM; b) 200-07-29, 29MM; c) 200-07-32, 32MM; d) 200-07-35, 35MM; e) 200-07-38, 38MM
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2151-2024·2024-06-26
Hospital bed mattress covers may delaminate from improper cleaning
Baxter Healthcare is recalling Centrella Max and Pro+ hospital bed mattresses that may develop delaminated top covers when cleaned with bleach-containing solutions. The mattresses prevent and treat pressure injuries.
Product
Centrella Max - The Centrella Smart+ Bed is intended for use in healthcare environments as a patient support system to prevent and/or treat pressure injuries.Multiple model numbers of Centrella Max mattresses and pro+ mattresses. (1) Centrella Max Surface, REF P7922A01; (2) C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2157-2024·2024-06-26
OPTETRAK Inset Patella knee implants recalled for improper vacuum packaging
Exactech is recalling OPTETRAK Inset Patella knee implants packaged in out-of-specification vacuum bags that may compromise product integrity during storage or sterilization.
Product
OPTETRAK Inset Patella, Item Numbers: a) 200-05-23, 23MM; b) 200-05-26, 26MM; c) 200-05-29, 29MM
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2155-2024·2024-06-26
Exactech Knee Patella Components Recalled Due to Out-of-Specification Vacuum Bags
Exactech is recalling OPTETRAK Three Peg Patella knee components packaged in out-of-specification vacuum bags. The affected products were distributed worldwide.
Product
OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-32, 32MM; d) 200-02-35, 35MM; e) 200-02-38, 38MM; f) 200-02-41, 41MM;
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2154-2024·2024-06-26
Bard Foley Catheter Trays Recalled for Temperature Display Malfunction
C.R. Bard Inc is recalling 6,420 Foley catheter trays nationwide because some devices may not display temperature readings or may display erratic readings. The malfunction could affect patient monitoring.
Product
Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection Control Temperature-Sensing Foley Catheter Tray with Bard Hydrogel and Bacti-Guard Silver Alloy Coating, 350 ml Urine Meter, 16 Fr, Catalog #319416AM. Intended
Category
Medical Device
Distribution
Distributed nationwide

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