electronic Recalls

325 recalls tagged with “electronic”.

Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed CareLink Clinic Recall 12,126 Units Worldwide in 2025

Medtronic MiniMed recalled 12,126 CareLink Clinic units worldwide after a software error misdisplays the 24-hour Sensor Glucose Overview Graph. The faulty software could prompt clinicians and patients to make therapy decisions based on incorrect glucose data. Patients should stop using the device immediately and contact Medtronic MiniMed or their healthcare provider for instructions.

Medtronic MiniMed
Software error
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Food & Beverages
HIGH
FDA FOOD

M.C.I. Foods Recalls 1,040 Cases of Ready-to-Eat Egg & Cheese Breakfast Burritos and Wraps (2025)

M.C.I. Foods recalled 1,040 cases of ready-to-eat Egg and Cheese Breakfast Burritos and Wraps sold to seven distributors nationwide for institutional use. A cooked egg ingredient used in the ready-to-eat products tested positive for Listeria monocytogenes. Consumers should not consume the product and should contact M.C.I. Foods for refund or replacement; notification will be by letter.

M.C.I. Foods
Cooked egg
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Health & Personal Care
HIGH
FDA DEVICE

DERMASENSOR DermaSensor 10101 Diagnostic Device Recalled for 9 of 343 Units (2025)

DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.

DERMASENSOR
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Glycar SA Recalls 18 SJM Pericardial Patch EnCap 5x10 cm REF C0510 in 2025 Recall

Glycar SA recalls 18 SJM Pericardial Patch with EnCap Technology 5x10 cm distributed in the US to healthcare facilities. The lot may not meet the required tensile strength specification. Stop use and follow manufacturer instructions provided by Glycar and your healthcare provider. Notification was issued by email.

Glycar SA
The impacted
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Recalled ESR HaloLock Kickstand Wireless Power Bank Model 2G505
HIGH
CPSC

ESR HaloLock Wireless Power Banks Recalled in Expansion to Include 2G505 Model for Fire and Burn Haz

ESR HaloLock wireless power banks were recalled in an expansion that now includes model 2G505. The recall covers models 2G520, 2G505B and 2G512B previously recalled and adds 2G505. The recall is distributed by Waymeet. The lithium-ion batteries can overheat and ignite. Consumers should stop using recalled power banks and seek a full refund from Waymeet.

ESR HaloLock
The lithium-ion
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella Controller Recall Aims to Address Cybersecurity Vulnerabilities Across 32 Product SK

Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.

Abiomed
Potential cybersecurity
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland 718096 Zenition 50 Interventional X-Ray System Recalled in 2025

Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
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Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Recalls 307 Cases of Cut Fresh Fruit Mix Over Listeria Risk (2025)

Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Mix due to potential Listeria monocytogenes contamination. The product was packed by WPS in Minneapolis, MN and distributed to five Midwest states. Consumers should not eat the recalled fruit and should contact the distributor for refund or replacement.

Wholesale Produce Supply LLC
Potential Listeria
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Health & Personal Care
HIGH
FDA DEVICE

Synthes 5.0mm IM Nail Screw Recalled for Labeling Error (2025)

Synthes USA recalled 122 locking intramedullary nail screws used in RFN-Advanced and Tibial Nail Advanced systems. The recall covers worldwide distribution including the US and Canada. The packaging labeling misstates screw length while the etched length on the screw is correct. Healthcare providers should stop using the device immediately and follow recall instructions from Synthes.

Synthes
Although the
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Food & Beverages
HIGH
FDA FOOD

Georgia Nut Co Recalls 76,121 Cases of tru fru Creme Freeze-Dried Strawberries 3.4 oz (2025)

Georgia Nut Co recalls 76,121 cases of tru fru Strawberries + Creme Freeze-Dried Fresh 3.4 oz pouches sold nationwide at retailers including Albertsons, CVS, Food Lion, H-E-B, Kroger, Target, Stew Leonard's and more. A potential for metal fragments in some packages is the hazard. Consumers should stop using the product and contact Georgia Nut Co for a refund or replacement.

Georgia Nut Co
potential for
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Health & Personal Care
HIGH
FDA DEVICE

BD BACTEC Blood Culture System Recall 1,086 Units Worldwide Over Unauthorized Access Risk (2025)

BD recalled 1,086 BD BACTEC Blood Culture System units worldwide after unauthorized access to product service credentials. The breach could compromise confidentiality, integrity and availability of affected devices and data. Hospitals and healthcare providers should stop using the device immediately and follow BD’s recall instructions.

BD
Product service
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Health & Personal Care
HIGH
FDA DEVICE

BD Phoenix M50 Recall: 4,283 Systems Worldwide Over Access Risk (2025)

BD recalled 4,283 Phoenix M50 Automated Microbiology Systems worldwide after unauthorized access to product service credentials. The unauthorized actor could access affected products and data. Labs should stop using these devices and follow the recall instructions from BD; contact BD for remediation guidance.

BD
Product service
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Health & Personal Care
HIGH
FDA DEVICE

BD Recalls 177 BACTEC Blood Culture System Units Over Unauthorized Access Risk (2025)

BD recalled 177 units of the BACTEC Blood Culture System worldwide after an unauthorized actor accessed product service credentials. The breach could allow unauthorized access to system configurations and data. Healthcare facilities should stop using the affected equipment and follow BD’s recall instructions.

BD
Product service
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Tag Statistics

Total Recalls
325

Related Tags

fda regulatedcpsc regulatedimmediate actionstop use immediatelyreturn for refundreplacement availableglassmetaladult producttoddler productchemical hazardelectrical hazard