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. 2,690 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,690 in last 12 months

Showing 2436124380 of 29,093 recalls

Medical DeviceAugust 6, 2014· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Anti-HCV Reagent Pack for in vitro...

The Issue: VITROS Immunodiagnostic Products Anti-HCV kit lot 9090 has been observed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Parker Laboratories, Inc.

Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...

The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Ellex iScience, Inc.

Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....

The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...

The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Arrow International Inc

Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...

The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Sedecal S.A.

Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...

The Issue: Reports of unexpected movement.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· Curbell Medical, Inc.

Recalled Item: CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor...

The Issue: The firm became aware of a potential problem that was initiated by a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· ICU Medical, Inc.

Recalled Item: Port Access Kit with MicroClave Clear Connector Recalled by ICU Medical,...

The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· ICU Medical, Inc.

Recalled Item: CAP Change Kit w/MicroClave Clear Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· ICU Medical, Inc.

Recalled Item: Cap Change Kit with MicroClave Clear Connector Recalled by ICU Medical, Inc....

The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2014· Catheter Connections, Inc.

Recalled Item: DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves Recalled by...

The Issue: Catheter Connections is recalling DualCap IV Pole Strips disinfectant caps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2014· Medical Components, Inc dba MedComp

Recalled Item: Split Cath III Trays Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2014· Civco Medical Instruments Inc

Recalled Item: CollectEVAC Recalled by Civco Medical Instruments Inc Due to A pinhole leak...

The Issue: A pinhole leak identified in the packaging of the recalled product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2014· Sorin Group USA, Inc.

Recalled Item: ST¿CKERT HeaterCooler System 3T Recalled by Sorin Group USA, Inc. Due to On...

The Issue: On August 1, 2014 Sorin Group USA, Inc. informed consignees via letter to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray V21 Recalled by Mindray DS USA, Inc. dba Mindray North America Due...

The Issue: Mindray DS USA Inc. initiated a voluntary field corrective action for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Roche cobas IT 1000 Product Usage: Intended Use: An electronic Recalled by...

The Issue: Potential that test results would be assigned to the wrong Patient ID if...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Carefusion 2200 Inc

Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...

The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing