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. 2,858 recalls have been distributed to Maryland in the last 12 months.
Showing 8281–8300 of 29,093 recalls
Recalled Item: (1) Gibeck Humid-Vent 2S Flex DC Recalled by TELEFLEX MEDICAL INC Due to...
The Issue: Reports received of torn corrugated breathing tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Teleflex Flex tube Recalled by TELEFLEX MEDICAL INC Due to Reports...
The Issue: Reports received of torn corrugated breathing tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer Recalled by Radiometer Medical ApS Due to Arterial Blood Sampler...
The Issue: Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL ReadiPlasTin Recalled by Instrumentation Laboratory Due to Variable...
The Issue: Variable and out of specification QC results with HemosIL ReadiPlasTin. IL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TMJ Arthroscopy Drape Recalled by Microtek Medical Inc. Due to Latex content...
The Issue: Latex content in product was labeled incorrectly as latex free.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoSight NS300 Recalled by MALVERN PANALYTICAL LTD Due to Product found to...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Resin UPDATE CD-ROM Recalled by Bio-Rad Laboratories, Inc. Due to The...
The Issue: The problem is with the Bio-Rad VARIANT nbs Sickle Cell Program Resin Update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Head Replacement System Implant is a one-piece Recalled by Synthes...
The Issue: DePuy Synthes Radial Head Replacement System Contraindications added to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accula SARS-CoV-2 Test Recalled by MESA BIOTECH, INC Due to SARS-CoV-2 Test...
The Issue: SARS-CoV-2 Test has an increased potential for false positive results, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRAY RING COVER Recalled by Johnson & Johnson Surgical Vision Inc Due to...
The Issue: Potential breach in the sterility barrier for tray ring covers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sara Plus Active Floor Lift Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due...
The Issue: The device may emit smoke or ignite.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The following first aid kits and cabinets containing components Medi-First...
The Issue: First aid kit and cabinet components are being recalled by the supplier due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Kit SARS-cCo V Antigen Rapid Test Recalled by USA Medical, LLC...
The Issue: COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 9100-Series Washer Disinfector models: 9120E Recalled by Getinge Usa...
The Issue: Inadequate documentation verifying whether device installation has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYSTO-URETHRO-FIBERSCOPE CYSTOSCOPE Recalled by Karl Storz Endoscopy Due to...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.