battery powered Recalls

293 recalls tagged with “battery powered”.

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recall: 60-Unit Anesthesia Tray Recalled for Catheter Connector Lid Position Issue

B BRAUN MEDICAL INC recalls 60 units of SESK Combined Spinal and Epidural Tray nationwide. The recall targets products distributed to all 50 states. The defective lid on the catheter connector may be in the incorrect position, posing a high-risk device issue. Stop using immediately and follow company instructions for recall remedies.

B BRAUN MEDICAL
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health 200 Salem Sump Gastroduodenal Tubes Recalled Worldwide for ARV Breakage

Cardinal Health 200, LLC recalled Salem Sump gastroduodenal tubes worldwide after reports of anti-reflux valve breakage. The ARV can fail under excessive force during use. Healthcare providers and patients should stop using the device immediately and follow the manufacturer instructions for recall communication.

Cardinal Health 200
Firm has
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Health & Personal Care
HIGH
FDA DEVICE

Fisher & Paykel Recall 51,144 Airvo 2 and myAirvo 2 Humidifiers Over Power-Disconnect Audible Alert

Fisher & Paykel Healthcare recalled 51,144 Airvo 2 and myAirvo 2 humidifiers in the United States. The devices may emit an audible alert for less than 120 seconds after power is disconnected. This could delay user awareness to reconnect power and lead to oxygen desaturation. Patients and healthcare providers should stop using the device and await manufacturer instructions.

Fisher & Paykel Healthcare
When unintentionally
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Health & Personal Care
HIGH
FDA DEVICE

Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)

Enterix recalled 201,426 InSure ONE Fecal Immunochemical Test kits after a sensitivity failure linked to Test Card Lot TT241102. The issue may cause false negative results. Healthcare providers and patients should stop using the affected kits and follow the manufacturer’s recall instructions.

Enterix
InSure ONE
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)

Baxter Healthcare recalled 5,209 oral/axillary probes used with Welch Allyn SureTemp Plus thermometers nationwide in the United States, Canada and Colombia. The probes were inadvertently programmed with the rectal configuration, which can yield a lower temperature reading. Healthcare providers and patients should stop using the affected probes immediately and follow Baxter’s recall instructions.

Baxter Healthcare
Affected oral/axillary
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Health & Personal Care
HIGH
FDA DRUG

IntegraDose Oxytocin IV Solution Recall 2025 for Subpotent Drug, 853 Bags Nationwide

IntegraDose Compounding Services recalled 853 IV bags of Oxytocin 30 Units/500 mL in 0.9% sodium chloride. The recall is nationwide in the United States. Testing found no oxytocin in the IV bags. Stop using the product and contact IntegraDose or a healthcare provider for guidance.

IntegraDose Compounding Services
Subpotent Drug:
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Health & Personal Care
HIGH
FDA DEVICE

Noah Medical Galaxy System GAL-001 Recall of 47 Units for Password-Protected Manual Access (2025)

Noah Medical recalled 47 Galaxy System bronchoscopic visualization devices distributed to 20 US states and internationally to Hong Kong and Australia. The recall centers on password-protected Instructions for Use. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

Noah Medical
Due to
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Recalled Bottle of Bariatric Fusion High ADEK Multivitamin
HIGH
CPSC

Blueroot Health Recalls Bariatric Fusion Iron Multivitamins Over Child Poisoning Risk (2025)

Blueroot Health recalled Bariatric Fusion iron multivitamin bottles after discovering the packaging is not child-resistant. The recall involves two bottle types with 45 mg of iron. Affected bottles lack the required push-down-and-turn caps and carry specific lot numbers. Consumers should stop using the product and contact Blueroot Health for a free child-resistant replacement cap.

Blueroot Health
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-P190 Bronchoscope Recall Updated for 2025 IFU Guidance

Olympus recalls 3,046 BF-P190 bronchovideoscopes sold nationwide in the US and 2,414 overseas. The recall centers on updated IFU guidance to clarify safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. Clinicians and facilities should stop using the device immediately and follow Olympus recall instructions.

Olympus
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-H190 Bronchovideoscope Recall Expanded for IFU Updates in 2025

Olympus Corporation of the Americas recalls 5,221 units sold in the U.S. and 4,321 units overseas. The recall covers the EVIS EXERA III BRONCHOVIDEOSCOPE BF-H190. It flags updated instructions for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. Patients and healthcare providers should stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific TENACIO Pump Recall 2025 for Inflation Deflation Issues

Boston Scientific recalled the TENACIO Pump without InhibiZone (UPN 72404420) worldwide, including the US and Canada. The device may experience inflation and/or deflation performance issues. Patients and healthcare providers should stop using the device immediately and follow the manufacturer's recall instructions.

Boston Scientific
The potential
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Cookies Recalled for Undeclared Red 40 and Yellow 6

Gina Marie Bakery LLC recalls Vanilla with Apricot Jam Cookies due to undeclared artificial colorings Red 40 and Yellow 6. The recall, initiated by the state of Connecticut and notified to the FDA, involves 172 cases at 20 containers per case. FDA-listed recall status is ACTIVE with no reported incidents yet.

Gina Marie Bakery
Undeclared Red
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Biscotti Recalled for Undeclared Red 40

Gina Marie Bakery LLC recalled 172 cases of Toasted Almond & Cherry Biscotti after the FDA flagged undeclared Red 40. The recall is classified as high hazard. Consumers should avoid the product and contact the company for refunds or replacements.

Gina Marie Bakery
Undeclared Red
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Health & Personal Care
HIGH
FDA DEVICE

NOXBOX Recalled 1,667 NOxBOXi Nitric Oxide Delivery System Units in 2025

NOXBOX recalled 1,667 NOxBOXi Nitric Oxide Delivery System units sold in Tennessee. The recall was issued Sept. 9, 2025. An internal fault can occur when users press the interface rapidly without waiting for the device to respond. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

NOXBOX
The unexpected
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare CSCS V3 MAS800 Central Station Recalled for 2,306 Units Worldwide (2025)

GE Healthcare recalled 2,306 CSCS V3 MAS800 Central Station desktops worldwide after identifying a software fault that can trigger a continuous reboot cycle. The issue can result in a loss of central monitoring for connected patients. Hospitals should stop using the affected devices and follow the recall instructions from GE HealthCare and Wipro GE Healthcare Private Ltd.

GE Healthcare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound L17-5 Transducer Recalled for Useful-Life Labeling (2025)

Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.

Philips Ultrasound
To provide
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Tag Statistics

Total Recalls
293

Related Tags

electrical hazardchemical hazardinfant productadult productteen productelderly productstop use immediatelyreturn for refundfda regulatednhtsa regulatedcpsc regulatedreplacement available