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. 2,760 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,760 in last 12 months

Showing 1940119420 of 29,093 recalls

Medical DeviceDecember 14, 2016· Ultradent Products, Inc.

Recalled Item: NanoTips 30g 20pk Recalled by Ultradent Products, Inc. Due to Ultradent...

The Issue: Ultradent Products, Inc. announces a voluntary field action for the NanoTips...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 12 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 16 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 16 mm [or 18 mm] Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT-X w/TrueV Upgrade Recalled by Siemens Medical Solutions USA...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Bio mCT-S(40) 3R->4R Upgrade Recalled by Siemens Medical Solutions USA Inc....

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT 20 Excel Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT X-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(64)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(64)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT X-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· MEDLINE IND

Recalled Item: Medline E-Z Lubricating Jelly Recalled by MEDLINE IND Due to Product was not...

The Issue: Product was not sterilized. Product was shipped to distribution centers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...

The Issue: Olympus has received complaints regarding the breakage of the endoscope's...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope Recalled...

The Issue: Olympus is recalling the URF-P6/P6R endoscopes due to a similar device...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Pentax of America Inc

Recalled Item: Rigid Laryngostroboscopes The Rigid Laryngostroboscopes Recalled by Pentax...

The Issue: Pentax is initiating a Field Correction to revise the Instructions for Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Great Basin Scientific, Inc.

Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...

The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...

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

Class II — Potential Health HazardOngoing