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. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 27221–27240 of 29,093 recalls
Recalled Item: x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm Recalled by Medtronic Xomed,...
The Issue: In March 2013, Medtronic issued a recall of the NIM TriVantage EMG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect QLC1677E Recalled by Steris Corporation Due to During a...
The Issue: During a routine label review, the firm identified four SYSTEM 1E Quick...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sepp Recalled by CareFusion 213, LLC Due to An internal review of...
The Issue: An internal review of CareFusion's labeling for preoperative skin prep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...
The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse...
The Issue: An internal protective fuse can be unintentionally activated while the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...
The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...
The Issue: Firm became aware of an unintended behavior when using the Mammomat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirtex SIR-yttrium 90 microspheres (Radionuclide) Recalled by Sirtex Medical...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...
The Issue: Medtronic has found through device testing that if the optional footswitch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Risk that air...
The Issue: Risk that air may be introduced into the device which may lead to an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...
The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.