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. 2,716 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,716 in last 12 months

Showing 2114121160 of 29,093 recalls

Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader Custom Lite Product Usage: Unloader Custom Lite is an Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Air Walker Product Usage: Rebound Air Walkers are indicated Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...

The Issue: After importing, the segmentation results appear mirrored at the CARTO...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Purewick Corporation

Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...

The Issue: PureWick is recalling external catheter for women Wicks because the labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Extreme Custom Product Usage: Extreme Custom is an external knee Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Miami J Collar Product Usage: Miami J collars are applied Recalled by Ossur...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced with BIOLINE Coating Custom tubing packs for the oxygenator...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Medtronic Inc.

Recalled Item: Reveal LINQ insertable Cardiac Monitor Recalled by Medtronic Inc. Due to...

The Issue: Medtronic has identified an issue with the sensitivity of an algorithm used...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Covidien Medical Products (Shanghai) Manufacturing L.L.C.

Recalled Item: Short Percutaneous Antenna with Thermosphere" Technology Standard...

The Issue: Medtronic is voluntarily recalling specific item codes and production lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Synthes (USA) Products LLC

Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: Out of specification at the thread. The thread height of these screws is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Synthes (USA) Products LLC

Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: Out of specification at the thread. The thread height of these screws is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM Receiver with Share Receiver Part Number: MT22495...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Custom Tubing Packs Custom tubing pack for oxygenators Recalled by Maquet...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· X-NAV Technologies, LLC

Recalled Item: X-Guide Surgical Navigation System Recalled by X-NAV Technologies, LLC Due...

The Issue: The X-Guide system utilizes an X-Clip (PN P007665) which contains fiducials...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Mako Surgical Corporation

Recalled Item: RESTORIS PST RIO Offset Shell Impactor For use by orthopedic Recalled by...

The Issue: Potential disassociation of the orientation pin.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver with Share Receiver Part Number:...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Professional) Receiver Receiver Part Number: MT20649...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i oxygenators Custom tubing packs for the oxygenator Recalled by...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL)...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing