Recalls published in June 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in June 2026, newest first.
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Class II · 5 months ago
Philips Azurion 7B12/12, Model Numbers: 722067 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
Daavlin Distributing Company Phothera 200, Phototherapy Devices indicated for use recall: Some of the Calibration/Output Certificates had the outputs reversed
Some of the Calibration/Output Certificates had the outputs reversed.
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Class I · 5 months ago
Kayserbetten Gmbh & Co. Kg Pediatric care bed recall: If the adjustment functions of the hand control
If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is…
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Class II · 5 months ago
Stryker Corporation Neptune Smart Docking Station recall: It has been identified that the impacted docking station (SN 2521008873)
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed…
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Class II · 5 months ago
Kico Knee Innovation Company Arvis Hip & Knee 3.0 Instrument Set recall: The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early
The 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 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
CareFusion 303, Inc. BD Pyxis Mini Main REF: 349 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
Intuitive Surgical, Inc. Brand Name: Da Vinci 5 Product Name: Assy,DV5 Tower recall: Due to unintentionally activated near infrared handheld camera
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions…
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Class II · 5 months ago
Philips Azurion 3M12, Model Numbers: 722063 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
Bayer Medical Care, Inc. Avanta Multi-Patient Administration Tube Sets ) used recall: Supplier changes resulted in a fit issue with the Contrast Flow Control Valve
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer…
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Class II · 5 months ago
CareFusion 303, Inc. BD Pyxis MedBank Tower REF: 1145-00 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¿Quincke Needle 26 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: Cesk Northside 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
Draeger, Inc. Atlan A350XL 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 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 I · 5 months ago
B Braun Medical Inc Spinocan Spinal Needle procedure kits: Material Description 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 I · 5 months ago
Becton Dickinson & Company BD¿Spinal Tray with BD¿Whitacre Needle 22 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 3M15, Model Numbers: 722064 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
B Braun Medical Inc Brand Name: B. Braun Medical INC. Product Name: Cesk Harris 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
Guardian Drug Co. Inc. Kirkland Signature, Ultra Strength Antacid, Calcium Carbonate recall: Presence of foreign substance: small metallic particles in chewable tablets
Presence of foreign substance: small metallic particles in chewable tablets.
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Class II · 5 months ago
Guardian Drug Co. Inc. Family Wellness, Ultra Strengt, Antacid Tablets recall: Presence of foreign substance: small metallic particles in chewable tablets
Presence of foreign substance: small metallic particles in chewable tablets.
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Class II · 5 months ago
Lannett Company Inc. Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles recall: Failed Dissolution Specifications: during 12M LT stability testing OOS low
Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.
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Class II · 5 months ago
Guardian Drug Co. Inc. Good Neighbor Pharmacy, extra strength Antacid Calcium recall: Presence of foreign substance: small metallic particles in chewable tablets
Presence of foreign substance: small metallic particles in chewable tablets.
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Class II · 5 months ago
Sun Pharmaceutical Industries Inc Xyvona , 3mg, 100 Tablets recall: Labeling: Not Elsewhere Classified. This recall has been initiated
Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary…