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. 2,782 recalls have been distributed to Maryland in the last 12 months.
Showing 17761–17780 of 29,093 recalls
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba...
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC-1000 Recalled by Panoramic Rental Corp. Due to The lift motor used to...
The Issue: The lift motor used to raise and lower the overhead chassis will wear if not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ReNew Reusable Grasper and Dissector Tips are to be Recalled by...
The Issue: The heat-shrink insulation tube may split during autoclave...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Cystoscope models ECY-1570 and ECY-1570K Recalled by Pentax of America...
The Issue: The video cytoscopes lack 510(k) premarket notification clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA...
The Issue: Instruments may, under certain specific circumstances listed below, fail to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP - Model 728311 Brilliance iCT - Model Recalled by Philips...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT - Model 728306 Computed Tomography X-ray systems Recalled by...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Purely Yours Breast Pump. Model 17070PMW and Model 17070ACA. Intended...
The Issue: Two specific lots was incorrectly manufactured containing a UK power adapter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondamed Biofeedback Device Recalled by Ondamed Inc Due to The firm was...
The Issue: The firm was marketing the Ondamed System in the US without marketing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit Recalled...
The Issue: Specific lots have been reported to produce falsely lower than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...
The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...
The Issue: Teleflex Medical is recalling the affected product because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.