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. 1,760 recalls have been distributed to Maryland in the last 12 months.
Showing 44821–44840 of 52,535 recalls
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The NAV3i Platform Power Box supplies the electrical components with...
The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...
The Issue: Sterility of the device may be compromised due to unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker NAV3i Platform is a mobile cart platform consisting Recalled by...
The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeVilbiss Model DV5x Series CPAP units. For use in treating Recalled by...
The Issue: A limited number of DV5x Series CPAP units were manufactured and shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products Calibrator Kit 17 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system...
The Issue: Although the Flat Panel Detector (FPD) touch sensor is activated during use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIPOTROPIC GOLD Recalled by John W Hollis Inc Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.