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. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 27941–27960 of 29,093 recalls
Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BariAir Therapy System The BariAir Therapy System is a risk Recalled by KCI...
The Issue: KCI has issued a medical device correction for the BariAir Therapy System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 400 system blood gas analyzer Product Usage: These...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿¿ 405 system blood gas analyzer Product PUsage: These...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 system blood gas analyzer Product Usage: RAPIDPoint...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1260 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1245 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1240 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1265 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS System versions 3.X and higher and 4.X and Recalled by Ge...
The Issue: There is a potential loss of image(s) associated with the Centricity to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy F/M Acetabular Shell without holes. Several ODs: 40MM Recalled by...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx E. coli/P. aeruginosa PNA FISH Recalled by Advandx Inc Due to...
The Issue: Some strains of Pseudomonas putida cross-react with the P. aeruginosa PNA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Acetabular AB Shells with Cluster Holes. The Trilogy Acetabular...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gish 3/8 x 3/8" Straight Connector with Luer fitting Recalled by Sorin Group...
The Issue: Due to a molding irregularity, certain lots of connectors have the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy F/M Acetabular Shell without holes SOLID HA. Several ODs: 38MM...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version...
The Issue: Fluoroscan Mini C-Arm models -InSight2, version 4.0 and 4.0.1 - DICOM images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minotrol 16 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: HORIBA Medical Irvine Technical Support received reports from some customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.