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 20041–20060 of 29,093 recalls
Recalled Item: RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod Recalled by...
The Issue: RTI Surgical Inc. (RTI) is conducting a voluntary recall on two specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle...
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 RX 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 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...
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: Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides...
The Issue: The firm sent the Technical Bulletin to consignees who received the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G 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: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G 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: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 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 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: Brivo XR385 Recalled by GE Healthcare, LLC Due to The placing of weight on...
The Issue: The placing of weight on the VRAD detector, of the Brivo XR385 digital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: Image data for a patients image may not be correct
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...
The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...
The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...
The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...
The Issue: Customers complained of low/empty reagent vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LipiFlow thermal Pulsation System Recalled by Tearscience, Inc Due to...
The Issue: Complaints related to an error condition occurring during patient treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...
The Issue: Two customer complaints suggest that excessive rotation of the cable in one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellman A CYNOSURE COMPANY Minor Surgery Bipolar Cable Recalled by Ellman...
The Issue: Mislabeling of the "expiration date". The expiration date on the outer box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Celerity ECG Cable Accessory Pack Recalled by Angiodynamics Inc. (Navilyst...
The Issue: The Celerity ECG Cable Accessory Pack has the potential to contain an ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System (Product Code ENGEN) configured with...
The Issue: Ortho confirmed that it is possible for the mis-association of sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.