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.

Agency

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

176–200 of 40175

ModerateFDA (Devices)·Z-0046-2027·2026-10-07
ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Product
Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 34" X 4" 2-Line, Blue Model/Catalog Number: ASP-564013 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0058-2027·2026-10-07
Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Product
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34" 2 LINE (10) Model/Catalog Number: DT-7034-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3313-2026·2026-10-07
Philips MR 7700 MRI Systems Recalled for Incorrect DTI Data Exports
Philips is recalling 107 MR 7700 MRI systems because diffusion tensor imaging (DTI) exports contain incorrect data, preventing accurate tractography reconstruction.
Product
MR 7700; Model number (REF): 1. 782120, 2. 782153, 3. 782155, 4. 782199; Software Versions: R11, R12 and R13;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0056-2027·2026-10-07
MPR Single Use Tourniquet Cuff Recalled for Incorrect Expiration Date
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Product
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 2 LINE (10) Model/Catalog Number: DT-7030-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3326-2026·2026-10-07
Micro Therapeutics Recalls Pipeline Flex Embolization Device Due to Labeling Error
Micro Therapeutics is recalling two units of the Pipeline Flex Embolization Device with Shield Technology because the packaging label incorrectly listed the diameter as 3.00 mm when the actual unit was 2.50 mm.
Product
Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex Embolization Device with Shield Technology consists of a permanent implant combined with a guidewire based delivery system. The Pipeline Flex Embolization…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0004-2027·2026-10-07
ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Product
Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number: 553323 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0063-2027·2026-10-07
Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global is recalling 80 MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
Product
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 2 LINE (10) Model/Catalog Number: DT-7112-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0065-2027·2026-10-07
ASP Global Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global, LLC. is recalling 180 units of MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Product
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 2 LINE (10) Model/Catalog Number: DT-7115-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0029-2027·2026-10-07
ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Product
Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-LINE (CS 18) YELLOW Model/Catalog Number: A70107008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3317-2026·2026-10-07
Philips MR 7700 Software Upgrade Recalled for Incorrect DTI Data
Philips is recalling 30 MR 7700 software upgrades because they export incorrect diffusion tensor imaging data, preventing accurate nerve fiber mapping.
Product
Upgrade to MR 7700; Model number (REF): 782130; Software Versions: R11, R12 and R13;
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3270-2026·2026-10-07
HeartSine Defibrillators Recalled for Missing Maintenance Supplement
HeartSine Technologies is recalling 31,834 public access defibrillators distributed without the required Maintenance Supplement, which describes an extra check every 3 months.
Product
HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, US English with…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3333-2026·2026-10-07
Karl Storz Recalls HOPKINS Telescope Eyepieces Due to Labeling Error
Karl Storz Endoscopy is recalling six HOPKINS Telescope eyepieces because of incorrect inside packaging labels. The units were distributed in Arizona, California, and Missouri.
Product
HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visualization of the surgical site during diagnostic and therapeutic endoscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-3194-2026·2026-09-30
AVID Medical Recalls Halyard IV Start Kits Due to Mold Contamination
AVID Medical is recalling Halyard IV Start Kits because they contain applicators potentially contaminated with Aspergillus penicillioides.
Product
Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3139-2026·2026-09-30
CooperSurgical Recalls Infant Nasal CPAP Tubing Due to Loose Connection Risk
CooperSurgical is recalling specific lots of INCA Infant Nasal CPAP tubing because a loose connection may cause loss of pressure and reduced oxygenation.
Product
INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-2707, 44-2709, 44-2710, 44-2712, 44-2715.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3266-2026·2026-09-30
Medline Neurological Sponges Recalled for Potential Endotoxin Variability
Medline Industries is recalling 128 Major Pack Convenience Kits containing neurological sponges due to potential endotoxin variability that may cause adverse health events.
Product
Medline Convenience Kits: 1) MAJOR PACK, Catalog Number: DYNJ81325A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3244-2026·2026-09-30
Olympus BiCOAG Hemostasis Probe Recall Due to Ceramic Tip Detachment Risk
Olympus is recalling 404 BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Product
Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3214-2026·2026-09-30
Boston Scientific Recalls Imager II Angiographic Catheters Due to Tip Fracture Risk
Boston Scientific is recalling Imager II Angiographic Catheters because the tip may fracture or detach, potentially causing device fragments to remain in or migrate through the patient's vasculature.
Product
Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M001314011 IMAGER II/5/ST/100/038 BX5; M001314021 IMAGER II/5/ST/65/035 BX 5; M001314031 IMAGER II/5/ST/100/035 BX 5; M001314041 IMAGER II/5/BARNH/100/038 BX5; M001314051 IMAGER…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3140-2026·2026-09-30
CooperSurgical Recalls Neonatal Nasal CPAP Replacement Sets Due to Loose Tubing
CooperSurgical is recalling 149 boxes of INCA Neonatal Nasal CPAP replacement sets because the flexible tubing may disconnect from the nasal cannula, potentially reducing treatment effectiveness.
Product
INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-0712, 44-0707, 44-0709, 44-0715.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3229-2026·2026-09-30
Medline Instrument Channel Brush Kits Recalled for Sharp Edges
Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.
Product
Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3245-2026·2026-09-30
Olympus BiCOAG Hemostasis Probe Recalled for Ceramic Tip Detachment Risk
Olympus is recalling 105 BiCOAG Hemostasis Probes because a manufacturing defect may cause the ceramic tip to detach during use.
Product
Olympus BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector. Model/Catalog Number: CD-B612LA.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3247-2026·2026-09-30
Olympus BiCOAG Hemostasis Probe Recalled for Potential Ceramic Tip Detachment
Olympus Corporation of the Americas is recalling 816 units of BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Product
Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3249-2026·2026-09-30
Philips EPIQ Elite Ultrasound System Recalled for Software Error
Philips is recalling 219 EPIQ Elite Diagnostic Ultrasound Systems due to a software issue that may cause inaccurate blood flow velocity measurements and potential misdiagnosis.
Product
Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3250-2026·2026-09-30
Becton, Dickinson ForeSight Elite Tissue Oximetry Cable Recall for Incorrect Channel Switching
Becton, Dickinson and Company is recalling 15,455 ForeSight Elite Tissue Oximetry Cables due to incorrect switching of Channel 1 and 2 on the module and flag labels.
Product
ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter cable is intended for use as an adjunct monitor of absolute regional hemoglobin oxygen saturation of blood under the sensors in individuals at risk for reduced…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3215-2026·2026-09-30
Heidelberg SPECTRALIS Flex Module Recall Due to Wheel Detachment Risk
Heidelberg Engineering is recalling 87 SPECTRALIS units with Flex Modules because wheels may detach, causing the stand to tip over and injure nearby people.
Product
Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module Model/Catalog Number: S3610, S2610, S2000, S1610 multimodal imaging platform optimized for the posterior segment of the eye
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3224-2026·2026-09-30
Maquet PowerLED 300 Concealed Lighting System Recalled for Detachment Risk
Maquet is recalling 667 PowerLED 300 Concealed Lighting Systems because the spring arm may detach and fall, posing a potential injury risk.
Product
PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2. ARD567501286;
Category
Medical Device
Distribution
Distributed nationwide

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176–200 of 40175