Recalls published in June 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in June 2026, newest first.
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Highest risk · 5 months ago
Hasuit 7-Drawer Dressers recall: The recalled dressers are unstable if they are not anchored to the wall
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious…
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Class II · 5 months ago
Baxter Healthcare Corporation Brand Name: Exacta Mix Product Name: Vented recall: Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron
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…
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Class II · 5 months ago
Philips Azurion 5M12, Model Numbers: 722227 with Software release recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class I · 5 months ago
B Braun Medical Inc Design Options Spinal Tray Spinal Needle Anesthesia procedure kits recall: These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a…
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Class II · 5 months ago
CareFusion 303, Inc. BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall: Fingerprint scanner may overheat to a temperature to cause 1st degree burn
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
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Class I · 5 months ago
Fresenius Kabi USA, LLC Ivenix Infusion System , Large Volume Pump recall: Fresenius Kabi has been made aware via customer complaints that dropping
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components…
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Class II · 5 months ago
B Braun Medical Inc Brand Name: B. Braun Medical INC. Product Name: Sesk Upmc Double recall: B. Braun was notified by our supplier, Ferndale Laboratories, Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary…
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Class II · 5 months ago
Windstone Medical Packaging, Inc. Aligned Medical AMS16835 Fluids Kit RX recall: Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
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Class II · 5 months ago
B Braun Medical Inc Brand Name: B. Braun Medical INC. Product Name: Cesk Riverside recall: B. Braun was notified by our supplier, Ferndale Laboratories, Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary…
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Class I · 5 months ago
Fresenius Kabi USA, LLC LVP software of the Ivenix Infusion System recall: Potential software anomaly that can cause the pump to report a false
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that…
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Class II · 5 months ago
CareFusion 303, Inc. BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall: Fingerprint scanner may overheat to a temperature to cause 1st degree burn
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
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Class I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 recall: This is a sub-recall of a product recall from Huons Co, Ltd
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…
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Class II · 5 months ago
B Braun Medical Inc Brand Name: B. Braun Medical INC. Product Name: Lyndon B Johnson recall: B. Braun was notified by our supplier, Ferndale Laboratories, Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary…
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Class II · 5 months ago
GE Medical Systems Information Technologies Inc CASE v7.0 Cardiac Testing System recall: Electrical sparking may occur at the printer head. If the Electrostatic
Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the…
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Class I · 5 months ago
Draeger, Inc. Atlan A350 recall: The Atlan anesthesia workstation either indicated a failure of the piston
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation…
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Class I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 recall: This is a sub-recall of a product recall from Huons Co, Ltd
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…
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Class II · 5 months ago
Philips Azurion 7B20/15, Model Numbers: 722068 recall: During the device phase of Roadmap Pro, a user may experience a dark image
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…
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Class II · 5 months ago
Covidien EndoStitch" Polysorb Single Use Loading Unit recall: The presence of holes in the pouch may compromise the package s ability
The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental…
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Class II · 5 months ago
Kico Knee Innovation Company Arvis Hip & Knee 2.0 Instrument Set recall: The Impactor V-Block Assembly and Trackers A, B
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.
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Class II · 5 months ago
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor recall: Temperature probe devices lack FDA clearance
Temperature probe devices lack FDA clearance.
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Class II · 5 months ago
Covidien Mon-a-Therm General Purpose recall: Temperature probe devices lack FDA clearance
Temperature probe devices lack FDA clearance.
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Class II · 5 months ago
CareFusion 303, Inc. BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall: Fingerprint scanner may overheat to a temperature to cause 1st degree burn
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
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Class II · 5 months ago
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus recall: Sterile wound dressing, lacks sterility assurance
Sterile wound dressing, lacks sterility assurance
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Class II · 5 months ago
SSC- Surgical Specialties Corporation Sharpoint 2.2MM, Angled, Double- Bevel Model/ recall: 3.0mm surgical knives labeled and packaged as 2.2mm surgical knives
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.