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. 2,898 recalls have been distributed to Maryland in the last 12 months.
Showing 1981–2000 of 52,535 recalls
Recalled Item: Tropicamide-Proparacaine-Phenylephrine-Ketorolac Recalled by Imprimis NJOF,...
The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine Lidocaine HCL Recalled by Imprimis NJOF, LLC Due to Sub-Potent...
The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...
The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...
The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics,...
The Issue: Generations 67 and above of VITROS Ca Slides are experiencing an increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator Recalled...
The Issue: Potential for the manometer port being blocked rendering the manometer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215....
The Issue: Label is incorrect. The product label indicates that the device contains an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ritz Peanut Butter Cracker Sandwiches Recalled by Mondelez Global Llc Due to...
The Issue: Undeclared allergens (Peanut) due to mispackaging
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ritz Peanut Butter Cracker Sandwiches Recalled by Mondelez Global Llc Due to...
The Issue: Undeclared allergens (Peanut) due to mispackaging
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ritz Cracker Sandwiches Recalled by Mondelez Global Llc Due to Undeclared...
The Issue: Undeclared allergens (Peanut) due to mispackaging
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ritz Peanut Butter Cracker Sandwiches Recalled by Mondelez Global Llc Due to...
The Issue: Undeclared allergens (Peanut) due to mispackaging
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vercise Deep Brain Stimulation Systems Surgical Implant Manual Recalled by...
The Issue: Wire break(s) have occurred in rechargeable deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Medline General Surgery Tray is customized to meet requirements Recalled...
The Issue: Affected kits contain recalled Stryker Color Cuff Sterile Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burr Hole Cover Kit Recalled by Boston Scientific Neuromodulation...
The Issue: Resistance and difficulties could occur while closing the retaining clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Infusion Sets Recalled by CareFusion 303, Inc. Due to...
The Issue: Infusion pump module used with compatible pump infusion sets may perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Module Model Recalled by CareFusion 303, Inc. Due to Infusion...
The Issue: Infusion pump module used with compatible pump infusion sets may perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.