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 9201–9220 of 29,093 recalls
Recalled Item: BF-XT160 EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08...
The Issue: When deleting a previously entered custom isotope, the software deletes the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-1T60 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-N20 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-P60 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-Q180-AC EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-XP160F EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-P180 EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.CT VA20A Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite with syngo.via VB30 Recalled by Siemens Medical...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A Recalled by...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imperative Care Recalled by IMPERATIVE CARE INC Due to There is a potential...
The Issue: There is a potential for distal end of catheters to fracture and become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring Recalled by Greiner...
The Issue: Blood collection tubes may experience a clotting issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Azurion series (within the limits of the used Operation Recalled by...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...
The Issue: Revised Instructions for Use: Potential for specimens from patients with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...
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: EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel Recalled by Red...
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: EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel Recalled by Red...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.