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Medical Device
FDA DevicesClass II

Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; ...

Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.

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

Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit 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.
Pharmaceutical
FDA DrugsClass I

Gas-X Extra Strength, SIMETHICONE 125 mg/ANTIGAS, packaged in a) 120 SoftGels (U...

Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.

Jun 17, 2026Haleon US Holdings LLC
auchan le poissonnier - crevettes cuites 50/70 equateur
RappelConsovolontaire (san...

auchan le poissonnier - crevettes cuites 50/70 equateur

présence de listeria monocytogenes (agent responsable de la listériose)

Jun 17, 2026auchan le poissonnier
Food & Beverage
Germany BVLGeneral Alert

Instantnudeln mit Hähnchengeschmack

Gesundheitsschädliche Substanz, Rückstände und Kontaminanten

Jun 17, 2026Importeur: Asia Express Food, Kilbystraat 1, 8263 Kampen, Niederlande Inverkehrbringer: Go Asia Deutschland GmbH, Kantstraße 115, 10627 Berlin Orient Master GmbH, Kantstraße 101, 10627 Berlin
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 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

SD LTM 64 PLUS, EEG Amplifier/recorder, Model/Catalog Number: SD LTM 64 PLUS, So...

Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier configuration (128 or 256 channels) running firmware version 2022.02 were displayed with a shift of 1 second between the 64channels blocks. In rare circumstances, a fixed 1-second temporal delay may appear between two 64-channel modules with firmware 2021.02, 2022.01 or 2022.02 in a multi-module SEEG configuration, potentially leading to misinterpretation of results.

Jun 17, 2026Micromed S.p.A.
Food & Beverage
FDA FoodClass II

Rollitos de DulceLeche [image] Caramel Rolls The Original, Net Wt. 15 oz, packag...

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

Jun 17, 2026Galaxy RG Corp
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

Allia Moveo 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

Halyard, Pain Pack. Kit Code: AMPK48-01.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

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

Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 3...

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

Cake de Fresa y Chocolate [image] Stawberry & Chocolate Cake The Original, Net W...

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

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

Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: ...

It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured. The potential clinical hazards include false or missed detection of M-protein (false positive); and falsely elevated or decreased M-protein concentration.

Jun 17, 2026The Binding Site Group, Ltd.
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
Food & Beverage
FDA FoodClass I

Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens M...

Contains undeclared allergen (shrimp).

Jun 17, 2026Kettle Cuisine, LLC
Medical Device
FDA DevicesClass II

Halyard, Eye Bag Pack. Kit Code: UIEB48-01.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Jun 17, 2026AVID Medical, Inc.
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
Pharmaceutical
FDA DrugsClass III

Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Ka...

Failed Impurities/Degradations Specifications

Jun 17, 2026Fresenius Kabi USA, LLC
Medical Device
FDA DevicesClass II

Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0....

Reusable electrodes may not meet expected performance levels.

Jun 17, 2026Boston Scientific Neuromodulation Corporation
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.
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