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. 2,877 recalls have been distributed to Maryland in the last 12 months.
Showing 5021–5040 of 29,093 recalls
Recalled Item: global Medium Recalled by CooperSurgical, Inc. Due to The firm has become...
The Issue: The firm has become aware of a sudden increase in complaints for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco MDSC-8527 NXF Recalled by Barco N.V. Due to Barco became aware of a...
The Issue: Barco became aware of a problem with I2C cables in the manufacturing process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acu-Loc and Acu-Loc 2 bone plates Recalled by Acumed LLC Due to Distribution...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory Sets Syringes: 6ml syringe with a female luer with Recalled by...
The Issue: Accessory sets contain a syringes not yet qualified for the accessory's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Medfusion Model 4000 syringe pump Recalled by Smiths Medical...
The Issue: Medfusion Model 4000 syringe infusion pumps, with the following software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PulseSpray Infusion System devices including: PULSE SPRAY 5F/135/20 Recalled...
The Issue: Rotating adaptor O-ring manufacturing defect impacting seal integrity which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...
The Issue: Reason for the voluntary recall is residue was identified on the two forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...
The Issue: When the catheters are used with the EnSiteX EP System, the system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...
The Issue: The jaw may fracture prior to the procedure during the inspection instructed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExcelsiusGPS Cannula A Recalled by Globus Medical, Inc. Due to Devices may...
The Issue: Devices may not be rendered sterile due to an internal gap that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total immunoglobulin M (IgM total) IVD Recalled by Siemens Healthcare...
The Issue: Potential for a negative bias with quality control (QC) and patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PANTHER FUSION System The Panther System is an Recalled by Hologic, Inc. Due...
The Issue: Due to potential false positive Flu B results when a sample was also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel Plus (Pneumoplus) Recalled by BioFire Diagnostics,...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500: Software Version 5.0 Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: A software issue that can incorrectly label all captured images that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.