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 9141–9160 of 29,093 recalls
Recalled Item: OPTETRAK LOGIC Polyethylene Tibial Inserts Recalled by Exactech, Inc. Due to...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX Recalled by...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRULIANT Knee System including TRULIANT Tibial Inserts Recalled by Exactech,...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System custom devices labeled as the following:...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System Recalled by Exactech, Inc. Due to Inserts...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION...
The Issue: When a measurement with a PTW detector array is performed with the software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part...
The Issue: Due to product not meeting specification for concentricity and failing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoLotion Transmission Lotion Recalled by North Coast Medical Inc Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norco Ultrasound Gel Recalled by North Coast Medical Inc Due to Ultrasound...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR450w 1.5T nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T SIGNA HDxt MR System nuclear magnetic resonance imaging system Recalled...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Creator Recalled by GE Healthcare, LLC Due to Under certain...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T nuclear magnetic resonance imaging system Recalled by...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Voyager nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.