FoodJun 17, 2026
Galaxy RG Cheesecake de Guava [image] Guava Cheesecake The Original, Net recall — FDA H-0936-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
Latest records
Latest recalls — page 32
The newest recall records with useful source details are listed here.
FoodJun 17, 2026
Galaxy RG Cake de Mango [image] Mango Cake The Original, Net Wt recall — FDA H-0926-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
FoodJun 17, 2026
Galaxy RG Cake de Fresa y Chocolate [image] Stawberry & Chocolate Cake recall — FDA H-0924-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
FoodJun 17, 2026
Galaxy RG Marquesita de Mango [image] Delighted Flavored Cakes The recall — FDA H-0929-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
FoodJun 17, 2026
Galaxy RG Tiramisu [image] Cofee Cake The Original, Net Wt recall — FDA H-0927-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
FoodJun 17, 2026
Galaxy RG Cheesecake de Fresa [image] Strawberry Cheesecake The recall — FDA H-0935-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
FoodJun 17, 2026
Galaxy RG Rollitos de DulceLeche [image] Caramel Rolls The Original, Net recall — FDA H-0920-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
FoodJun 17, 2026
Galaxy RG Rollitos de Guava [image] Guava Rolls The Original, Net Wt recall — FDA H-0919-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
FoodJun 17, 2026
Galaxy RG Marquesita de Chocolate y Vainilla [image] Delighted Flavored recall — FDA H-0932-2026
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Class IIFDA: OngoingGalaxy RG Corp
Medical DeviceJun 10, 2026
Exacta Mix Vented Micro-Volume Inlet recall — FDA Z-2262-2026
Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slower…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJun 10, 2026
Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3 recall — FDA Z-2286-2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceJun 10, 2026
B Braun Medical Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material recall — FDA Z-2278-2026
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential…
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall — FDA Z-2302-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
Fresenius Kabi USA Ivenix Infusion System (IIS), Large Volume Pump recall — FDA Z-2224-2026
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily…
Class IFDA: OngoingFresenius Kabi USA, LLC
Medical DeviceJun 10, 2026
B. BRAUN MEDICAL INC. SESK UPMC DOUBLE CATHETER TRAY recall — FDA Z-2270-2026
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the…
Class IIFDA: OngoingB Braun Medical Inc
Medical DeviceJun 10, 2026
B. BRAUN MEDICAL INC. CESK RIVERSIDE HEALTH SYSTEM recall — FDA Z-2268-2026
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the…
Class IIFDA: OngoingB Braun Medical Inc
Medical DeviceJun 10, 2026
Fresenius Kabi USA LVP software of the Ivenix Infusion System (IIS) recall — FDA Z-2223-2026
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is…
Class IFDA: OngoingFresenius Kabi USA, LLC
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall — FDA Z-2304-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
Becton Dickinson & Company BDSpinal Tray with BDWhitacre Needle 25 G x 3.5 in recall — FDA Z-2256-2026
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during…
Class IFDA: OngoingBecton Dickinson & Company
Medical DeviceJun 10, 2026
B. BRAUN MEDICAL INC. LYNDON B JOHNSON HOSPITAL SPINAL EPID recall — FDA Z-2267-2026
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the…
Class IIFDA: OngoingB Braun Medical Inc
Medical DeviceJun 10, 2026
GE Medical Systems Information Technologies CASE v7.0 Cardiac Testing System Model no. recall — FDA Z-2279-2026
Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or…
Class IIFDA: OngoingGE Medical Systems Information Technologies Inc
Medical DeviceJun 10, 2026
Draeger Atlan A350 recall — FDA Z-2207-2026
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Class IFDA: OngoingDraeger, Inc.
Medical DeviceJun 10, 2026
Becton Dickinson & Company BDSpinal Tray with BDWhitacre Needle 24 G x 3.5 in recall — FDA Z-2252-2026
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during…
Class IFDA: OngoingBecton Dickinson & Company
Medical DeviceJun 10, 2026
Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1 recall — FDA Z-2289-2026
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026145 records · 4 categoriesJuly 2026366 records · 4 categoriesJune 2026368 records · 4 categoriesMay 2026328 records · 4 categoriesApril 2026405 records · 4 categoriesMarch 2026171 records · 4 categoriesFebruary 2026121 records · 4 categoriesJanuary 202662 records · 3 categoriesDecember 2025101 records · 3 categoriesNovember 202596 records · 3 categoriesOctober 2025133 records · 3 categoriesSeptember 2025116 records · 3 categories