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. 2,716 recalls have been distributed to Maryland in the last 12 months.
Showing 22081–22100 of 29,093 recalls
Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted...
The Issue: The firm has received 15 complaints over ten years related to the connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended Recalled...
The Issue: It was discovered that the above part number and lot of 2.4mm Locking Screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RBT Recalled by BioHorizons Implant Systems Inc Due to An incorrect label...
The Issue: An incorrect label reading 10.5mm and not the specified 15mm was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Computed Tomography X-ray system Recalled by Philips...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rainbow Reusable Sensors. RAINBOW DCI-DC3 Recalled by Masimo Corporation Due...
The Issue: These sensors were manufactured with incompatible configurations. This could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DA-2006P - Defibrillator / Pacer Analyzer Recalled by BC Group International...
The Issue: Device is not functioning as intended: Two wires running to the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Perfusion Tubing Packs Recalled by Medtronic Perfusion Systems Due...
The Issue: This recall is being initiated due to a potential breach of the Tubing Pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProTrack Microcatheter. Model/Catalog Numbers CIC38-145 Recalled by Baylis...
The Issue: Microcatheter may have circumferential defects (cracks) along its shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.