Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,864 recalls have been distributed to Maryland in the last 12 months.
Showing 6741–6760 of 29,093 recalls
Recalled Item: ARTIS one with a hybrid cable- An angiography system developed Recalled by...
The Issue: Examination room monitor connected with the hybrid cable may have a display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813...
The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814...
The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DERMLITE DL4W Recalled by DermLite LLC Due to Incorrect labeling; Package...
The Issue: Incorrect labeling; Package labeling contains a different serial number then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...
The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery....
The Issue: Device suddenly and forcefully disassembled after cryotherapy, potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SenSight Extension Tunneler Kit Recalled by Medtronic...
The Issue: Medtronic has received reports of SenSight Extension Tunneler kits that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integre Pro Yellow LP561 Recalled by Ellex Medical Pty Ltd. Due to When...
The Issue: When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Cortisol 50T (Material Number 10995538) Recalled by Siemens...
The Issue: There is a negative bias with urine patient samples and urine cortisol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Cortisol 50T (Material Number 10994924) Recalled by Siemens...
The Issue: There is a negative bias with urine patient samples and urine cortisol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Carefusion V. Mueller Graves Vaginal Speculum Recalled by Carefusion...
The Issue: A portion of the two products were incorrectly marked (etched) and packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JULIET Ti LL Recalled by SPINEART SA Due to JULIET Lateral Lumbar Ti-Life...
The Issue: JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Access Free T3 Recalled by Beckman Coulter, Inc. Due to The...
The Issue: The reagent lot produces elevated results (approximately >30%) in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF) Recalled by...
The Issue: Potential shearing of the disposable blade may occur and be contained within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-C6 Recalled by Hamilton Medical AG Due to Software error causes,...
The Issue: Software error causes, safety ventilation, in which ventilation continues in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum Perfusion Systems for CPB Recalled by Spectrum Medical Ltd. Due to...
The Issue: The ratchet and pawl had an out of tolerance geometry which exhibited as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System- For use in the in vitro quantitative Recalled...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System - For use in the in vitro quantitative...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.