United States Recalls

Consumer recalls from the FDA, CPSC, NHTSA, and USDA FSIS.

Showing 24 of 16,529 results
Medical Device
FDA DevicesClass II

Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number...

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Jun 17, 2026Avanos Medical, Inc.
Food & Beverage
FDA FoodClass II

Marquesita de Guava [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz...

Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

Jun 17, 2026Galaxy RG Corp
Medical Device
FDA DevicesClass II

Allia IGS 5 Pulse angiographic X-ray system

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.

Jun 17, 2026GE Medical Systems, LLC
Medical Device
FDA DevicesClass II

CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND093...

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Jun 17, 2026INSPIREMD Inc
Medical Device
FDA DevicesClass II

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUS...

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Jun 17, 2026Avanos Medical, Inc.
Medical Device
FDA DevicesClass II

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit ...

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Jun 17, 2026Avanos Medical, Inc.
Medical Device
FDA DevicesClass II

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

Jun 17, 2026Philips North America Llc
Medical Device
FDA DevicesClass II

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUL...

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Jun 17, 2026Avanos Medical, Inc.
Medical Device
FDA DevicesClass II

Hintermann Series Talar Implant, Left, Size 2 REF 302112

Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.

Jun 17, 2026DT MedTech, LLC
Medical Device
FDA DevicesClass II

Plum Solo Precision IV Pump, 40001-0401

Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.

Jun 17, 2026ICU Medical, Inc.
Medical Device
FDA DevicesClass II

NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Prod...

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

Jun 17, 2026In2bones USA, LLC
Medical Device
FDA DevicesClass II

Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180

Sterile anchors my lack sterility assurance.

Jun 17, 2026Boston Scientific Neuromodulation Corporation
Medical Device
FDA DevicesClass II

Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog N...

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Jun 17, 2026INSPIREMD Inc
Medical Device
FDA DevicesClass II

Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPO...

Due to incorrect incubation process being performed on product.

Jun 17, 2026HF Acquisition Co LLC
Food & Beverage
FDA FoodClass II

Rollitos de Guava [image] Guava Rolls The Original, Net Wt. 15 oz, packaged in a...

Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

Jun 17, 2026Galaxy RG Corp
Medical Device
FDA DevicesClass II

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUS...

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Jun 17, 2026Avanos Medical, Inc.
Medical Device
FDA DevicesClass II

Allia IGS 3 Pulse angiographic X-ray system

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.

Jun 17, 2026GE Medical Systems, LLC
Medical Device
FDA DevicesClass II

Bicarby Dialysate; Model number: RFP-400-G;

There is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the product correctly identifies the product code and the solution contained in the bag. In the event the incorrect GTIN labeling is used as the singular source for product identification, unrecognized use of a potassium solution with a concentration differing from the prescription may result.

Jun 17, 2026Fresenius Medical Care Holdings, Inc.
Medical Device
FDA DevicesClass II

Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL...

Reusable electrodes may not meet expected performance levels.

Jun 17, 2026Boston Scientific Neuromodulation Corporation
Vehicle
NHTSAELECTRICAL SYSTEM

Storyteller Overland - Alternator Pulley Failure May Cause Power Brakes and Powe...

An unexpected loss of power brakes increases the distance required to stop. A loss of power steering increases the amount of effort needed to control the vehicle. Both situations may increase the risk of a crash.

Jun 16, 2026Storyteller Overland
Vehicle
NHTSAEQUIPMENT

Forest River, Inc. - Incorrect GVWR on Certification Label/FMVSS 120

Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Jun 15, 2026Forest River, Inc.
Safety Alert
RSS FeedGeneral Alert

Western Mixers Produce & Nuts Issues Allergy Alert on Undeclared Peanuts in First Street Brand, Dark Chocolate Raisins

Jun 15, 2026
Vehicle
NHTSASTRUCTURE

Wabash National Corporation - Insufficient Rear Impact Protection/FMVSS 223

An improperly installed guard may not sufficiently protect a following vehicle, increasing the risk of injury during a rear end crash.

Jun 15, 2026Wabash National Corporation
Vehicle
NHTSAELECTRICAL SYSTEM

Waymo LLC - Software May Allow Vehicle to Enter and Drive In Freeway Constructio...

Driving through a closed construction zone increases the risk of a crash.

Jun 13, 2026Waymo LLC
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