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. 2,760 recalls have been distributed to Maryland in the last 12 months.
Showing 19121–19140 of 29,093 recalls
Recalled Item: Influenza Transport Swab Packages Recalled by Quidel Corporation Due to...
The Issue: Quidel Corporation is recalling Influenza Transport Swab Packages because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS HI and Mevatron M2/Primus Mid-Energy Recalled by Siemens Medical...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UNI-CP System Recalled by Integra LifeSciences Corp. Due to The firm...
The Issue: The firm received one complaint from one non-US sales representative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON MD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6730/6740 (MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON KD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6700 (MX) Accelerator Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) Recalled...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Drape Recalled by Covidien LLC Due to Sterility compromised...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XTRAC Excimer Laser Recalled by Strata Skin Sciences, Inc. Due to When the...
The Issue: When the Liquid Guide ( LLG) is not used according to the operator manual,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR450 The systems are whole body magnetic resonance scanners...
The Issue: Potential safety issue with the patient bore heating on the Discovery MR450...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cadence Total Ankle System Recalled by Integra LifeSciences Corp....
The Issue: Posterior tibial fractures have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CaviWipes1 Extra Large Recalled by Metrex Research, LLC. Due to Metrex is...
The Issue: Metrex is recalling the CaviWipes Extra Large because they may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN Recalled by Argon Medical...
The Issue: The recalling firm received a complaint from one of their customers of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST XM256 (Cefuroxime) Recalled by BioMerieux SA Due to Potential...
The Issue: Potential performance issues. False Susceptible result instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.