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. 2,727 recalls have been distributed to Maryland in the last 12 months.
Showing 20021–20040 of 29,093 recalls
Recalled Item: OEC Brivo 715 Prime Recalled by GE OEC Medical Systems, Inc Due to GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC Brivo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waste Management Kit. Catalog Number K10-04381AP Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA 27 Microcatheter Recalled by Sequent Medical Inc Due to Sequent Medical...
The Issue: Sequent Medical is recalling the VIA 27 Microcatheter because it may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluid Management Set. Catalog Number K08-MP5159A Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A Recalled by Merit...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold Kit. Catalog Number K09-11867AP Recalled by Merit Medical Systems,...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog...
The Issue: O-arm O2 Surgical Imaging System Spatial calibration may be erroneous in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBRA Fusion 50 Ablation System Recalled by AtriCure, Inc. Due to Due to...
The Issue: Due to product design and process control, part of the device can separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product...
The Issue: There is a potential for a component failure of the device which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD79b PE (ASR) Recalled by Becton, Dickinson and Company, BD Biosciences Due...
The Issue: CD79b (SN8) PE is contaminated with a FITC conjugate of unknown antigenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee System Box Cut Guide The EMPOWER PS Recalled by Encore...
The Issue: It has been discovered that during Empowr PS Total Knee replacement, while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or...
The Issue: Issue with the process for detection of leaking Pressure Tourniquet Cuffs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PeroxiClear Peroxide Solution Recalled by Bausch & Lomb Inc Irb Due to...
The Issue: Product was found to contain excess residual levels of hydrogen peroxide.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass .023" Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.