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. 2,685 recalls have been distributed to Maryland in the last 12 months.
Showing 26401–26420 of 29,093 recalls
Recalled Item: Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue...
The Issue: Blue Belt Technologies is recalling sterile Monitor Drapes used with their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR V-Patch Mesh (All sizes and shapes). Intended for use Recalled by...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-QUR TacShield Mesh (All sizes and shapes). Intended for use Recalled by...
The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...
The Issue: Siemens has become aware of a customer complaint concerning the rail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Temperature Probes Recalled by Vital Signs Devices, a GE...
The Issue: GE Healthcare has become aware of a potential safety issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distributed in USA: Product Number: 40-2894: Reinforced Wound Closure...
The Issue: Aspen Surgical is recalling Wound Closures because firm could not confirm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is labeled in part: LIST NO. 43449 Recalled by Hospira Inc. Due to...
The Issue: Hospira has recieved reports that the vacuum needed to create suction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion System. Model Numbers: 1D80R8 Recalled by...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion System with Trillium BioSurface (a polymer...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PleuraGuide Disposable Chest Tube Kit Recalled by Atrium Medical Corporation...
The Issue: Individual component's IFUs are not included with the kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProTime Microcoagulation System Recalled by Assuramed Due to The products...
The Issue: The products may have been stored at temperatures outside their required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT and Brilliance iCT SP These systems are intended Recalled by...
The Issue: An artifact that resembles thrombus may appear on the image.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAC Pneumatic Retraction Arm. A support arm used to hold Recalled by...
The Issue: Changes were implemented to the UNITRAC instructions for use to ensure safe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemoccult II BRAND SENSA elite Recalled by Assuramed Due to The products may...
The Issue: The products may have been stored at temperatures outside their required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid...
The Issue: The products may have been stored at temperatures outside their required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.