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
June 2026 recalls — page 11
These records include useful source details for the selected month.
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.
Medical DeviceJun 10, 2026
Covidien EndoStitch" Polysorb Single Use Loading Unit recall — FDA Z-2281-2026
The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.
Class IIFDA: OngoingCovidien, LP
Medical DeviceJun 10, 2026
Kico Knee Innovation Company Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing recall — FDA Z-2293-2026
The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Class IIFDA: OngoingKico Knee Innovation Company
Medical DeviceJun 10, 2026
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042 recall — FDA Z-2271-2026
Temperature probe devices lack FDA clearance.
Class IIFDA: OngoingCovidien LLC
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall — FDA Z-2297-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
SSC- Surgical Specialties Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL recall — FDA Z-2309-2026
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
Class IIFDA: OngoingSSC- Surgical Specialties Corporation
Medical DeviceJun 10, 2026
Shimadzu Medical Systems Digital Angiography System Trinias:UD150G-40 / D150GC-40 recall — FDA Z-2294-2026
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
Class IIFDA: OngoingShimadzu Medical Systems
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall — FDA Z-2299-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.