Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,278 results
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.
Medical Device
FDA DevicesClass II

CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1...

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

Jun 17, 2026INSPIREMD 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

EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ...

Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.

Jun 17, 2026BERLIN HEART GMBH
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

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.
Safety Alert
Health CanadaType II

HALYARD* PUREZERO* Ultraviolet* Nitrile Exam Gloves

Performance

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

Cake de Capuchino [image] Capuchino Cake The Original, Net Wt. 63 oz, packaged i...

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

Jun 17, 2026Galaxy RG Corp
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

Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannu...

The cannulation of the CCS screw is not centered.

Jun 17, 2026Medartis AG
Food & Beverage
FDA FoodClass II

NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL,...

Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.

Jun 17, 2026SENSORY SUPPLEMENT LLC
Food & Beverage
FDA FoodClass II

Brazo Gitano [image] Caramel Sweet Roll The Original, Net Wt. 24 oz, packaged in...

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
Food & Beverage
FDA FoodClass II

Marquesita de Mango [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
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
Food & Beverage
FDA FoodClass II

Capuchino [image] Syrup Cone Cake The Original, Net Wt. 13 oz, packaged in a tra...

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 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.
Pharmaceutical
FDA DrugsClass III

Primidone Tablets, USP, 50 mg, 100 Tablets per Bottle, Rx only, Manufactured by:...

Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.

Jun 17, 2026Amneal Pharmaceuticals, LLC
Food & Beverage
FDA FoodClass II

Jumbo Brazo Gitano Caramelo [image] Jumbo Caramel Roll The Original, Net Wt. 40 ...

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

Jun 17, 2026Galaxy RG Corp
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
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

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

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
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