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. 2,702 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,702 in last 12 months

Showing 2312123140 of 29,093 recalls

Medical DeviceApril 20, 2015· ICU Medical, Inc.

Recalled Item: 104" (264 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...

The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· ICU Medical, Inc.

Recalled Item: 98" (249 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...

The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· ICU Medical, Inc.

Recalled Item: 107" (272 cm) Ext Set w/2 Check Valves Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2015· Zimmer CAS

Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...

The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2015· Biosense Webster, Inc.

Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...

The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2015· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...

The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2015· Spacelabs Healthcare Inc

Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...

The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Delivery/C-Section Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Covidien Devon Light Gloves Recalled by Covidien LLC Due to Devon Light...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Surgical Kit Sterile-Kits containing the Devon Light Glove Catalog...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Mini-Kits Recalled by Covidien LLC Due to Devon Light Gloves contain splits...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Hysto Pack Recalled by Covidien LLC Due to Devon Light Gloves contain splits...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Wright Medical Technology, Inc.

Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....

The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: MCK Maximum Congruent Knee System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Minor Surgical Kits Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Single Basin Kits Recalled by Covidien LLC Due to Devon Light Gloves contain...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: NS-3600-B LITE GLOVE 1000/CASE -Bulk Recalled by Covidien LLC Due to Devon...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing