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 28301–28320 of 52,535 recalls
Recalled Item: Conversion SmarthPath to dStream for 1.5T Recalled by Philips Electronics...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...
The Issue: The product label has missing information, such as the lot number and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rectal Catheters Recalled by Teleflex Medical Europe Ltd Due to These...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a)...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URO-3 Triple Stain (CD44 + p53) with CK20 Recalled by Biocare Medical, LLC...
The Issue: Immunohistochemistry device kits found to display incorrect staining pattern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Alka-Seltzer Plus¿ packages with a full front panel instant Recalled by...
The Issue: Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision Recalled by...
The Issue: After continuous operation for more than one and a half days, the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...
The Issue: The cap on the vial might be labeled with the incorrect part number but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx AED. Recalled by Philips Electronics North America...
The Issue: An issue with one of the electric components (a resistor) could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.