replacement available Recalls

1,215 recalls tagged with “replacement available”.

Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalled 125 Imactis CT-Navigation System Stereotaxic Accessories in 2026

GE Medical Systems recalled 125 Imactis CT-Navigation System stereotaxic accessories distributed worldwide to healthcare facilities. The recall cites a potential mismatch between the simulated needle trajectory and the actual trajectory. Healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.

GE Medical Systems
There is
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Vehicles & Parts
HIGH
NHTSA

Mazda CX-50 Trailer Hitch Recall Affects 2024-2025 SUVs

Mazda North American Operations is recalling certain 2024-2025 CX-50 SUVs equipped with Mazda Genuine Accessory trailer hitches sold through Mazda dealerships. The recall number is 7225C and owner notification letters were mailed April 4, 2025. The recall addresses bolts that may loosen and detach the hitch. Owners should contact their Mazda dealer to schedule a free tightening.

Mazda
A detached
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Vehicles & Parts
HIGH
NHTSA

Ford Explorer 2026 Recall for Transmission Valve Body Issue

Ford recalls 2024-2025 Explorer and other models for a transmission valve body defect. The valve body may have been machined incorrectly, causing reverse gear failure or unexpected forward movement in reverse or neutral. Owner notification letters were mailed April 11, 2025; dealers will replace the valve body at no charge.

Ford
Unexpected vehicle
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe Ergo 321-09-05 Impactor Handle Recall (120 Units, 2026)

Exactech recalled 120 Equinoxe Ergo Modular Impactor Handles after identifying a missing cross-pin. The defect could compromise instrument integrity during surgical use. Hospitals and surgeons should stop using the devices immediately and follow Exactech's recall instructions.

Exactech
Impactor handle
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Health & Personal Care
HIGH
FDA DEVICE

Ion Beam Applications PROTEUS 235 Recalled for 4 Units Worldwide (2026)

Ion Beam Applications S.A. recalled four PROTEUS 235 proton therapy systems distributed worldwide, including Florida in the United States, and the countries of Italy and Japan. The defect disables the Therapy Safety System's Universal Beam Triggering Interface, so the system may not stop beam delivery if the Healthy Signal from an external gating device is lost. Patients and healthcare providers应该

Ion Beam Applications
It was
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical 21GA Winged Infusion Set 7M2802 Recalled 51,300 Units (2026)

B. Braun Medical recalls 51,300 units of its 21GA Winged Infusion Set, model 7M2802, distributed worldwide including Texas and Costa Rica. The device’s needle tip can be dull or break, making advancement difficult. Stop using the device immediately and contact the manufacturer or your healthcare provider for instructions.

B. Braun Medical
The potential
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 21GA Winged Infusion Set (7A3842) 21,000 Units (2026)

B. Braun Medical is recalling 21,000 21GA Winged Infusion Sets (Single Pack) distributed worldwide, including Texas and Costa Rica, catalog 7A3842. The needle tip can be dull or blunt, may be difficult to advance, or break. Clinicians and patients should stop using the device and await manufacturer instructions.

B. Braun Medical
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Insulin Infusion Pumps Recalled 1,380 Units in 2026 Over Czech Guide Error

Tandem Diabetes Care recalled 1,380 insulin infusion pumps distributed internationally in the Czech Republic and Slovakia after translation errors in the Czech user guide could cause unintended insulin delivery. The most significant error told users to verify the infusion set is connected to the body when it should be confirming it is not connected. Following this instruction could result in a hyp

Tandem Diabetes Care
The Czech
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 780G Recall 2026: 26,851 Pumps Hit Over Software Defects

Medtronic MiniMed recalled 26,851 MiniMed 780G insulin pumps sold worldwide, including the United States and Israel. Three software defects tied to updates 6.60, 6.61, and 6.62 could misdose insulin. Stop using the affected pumps and follow the recall letter for instructions.

Medtronic MiniMed
Three software
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter AU5800 Chemistry Analyzer Recall for 47 Units Over Calibration Delay Issues (2026)

Beckman Coulter Mishima K.K. recalled 47 AU5800 chemistry analyzers sold nationwide in the United States after a software delay can cause calibration and reagent databases to fail to open. The issue occurs when a calibration monitor using Microsoft SQL Server 2022 Express remains open for more than 15 minutes, potentially halting analysis. Healthcare facilities should stop using the devices and (a

Beckman Coulter
A delay
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Health & Personal Care
HIGH
FDA DEVICE

Medline Chest Drainage Units Recall Updated IFUs for Adults 18+

Medline Industries recalls 2,894 Aqua-Seal Chest Drainage Units from Cardinal Health after updating IFUs to specify adult patients 18 years and older. The devices were distributed worldwide, including California, Chile and Panama. The update clarifies intended patient population and requires action from healthcare providers to stop use until further notice.

Medline Industries, LP
The instructions
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Health & Personal Care
HIGH
FDA DEVICE

Paradise Renal Denervation Catheter Recalled for 1 Unit in 2026

Paradise Renal Denervation Catheter was recalled after a single unit distributed nationwide in nine states was deemed nonconforming and not for human use. The device is an ultrasound renal denervation catheter. Healthcare providers should stop using it and contact ReCor Medical for instructions.

Paradise
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-210 Single-Use Biopsy Valve Recalled for 95,882 Boxes Nationwide (2026)

Olympus Corporation of the Americas recalls 95,882 boxes of MAJ-210 single-use biopsy valves distributed nationwide to hospitals and clinics in the United States after reports of rubber fragments detaching during use. The defect can release fragments into the endoscope channel or patient. Healthcare facilities should stop using the device immediately and follow recall instructions.

Olympus
Potential for
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 200 mg Recall Affects 19,056 Bottles Nationwide (2026)

Teva Pharmaceuticals recalled 19,056 bottles of Metoprolol Succinate Extended-Release Tablets, 200 mg, sold nationwide. The recall cites failed dissolution specifications, which could affect how the drug releases in the body. Patients should stop using the product and contact Teva or their healthcare provider for guidance.

METOPROLOL SUCCINATE
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 50 mg Extended-Release Recall 2026 Following Failed Dissolution Specs (67,

Teva Pharmaceuticals recalled 67,043 bottles of Metoprolol Succinate Extended-Release Tablets, 50 mg, distributed nationwide. The FDA enforcement report cites Failed Dissolution Specifications as the hazard. Health care providers and patients should stop using this product immediately and contact Teva for guidance.

METOPROLOL SUCCINATE
Failed Dissolution
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Tag Statistics

Total Recalls
1,215

Related Tags

fda regulatedcpsc regulatedimmediate actionstop use immediatelyreturn for refundelectronicbattery poweredworkplacevehiclemetalrepair availablenhtsa regulated