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. 2,590 recalls have been distributed to Maryland in the last 12 months.
Showing 42521–42540 of 52,535 recalls
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops A.C. (Tetrahydrozoline HCl 0.05% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops Advanced Relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops (Tetrahydrozoline HCl 0.05%) Recalled by K C Pharmaceuticals Inc...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops Industrial Strength (Polyethylene glycol 400 1% Recalled by K C...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...
The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...
The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...
The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...
The Issue: Failed Stability Specifications: Product is subpotent and has out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotoprone Therapy System. The Rotoprone Therapy System is an advanced...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Artifacts are found in acquired imaging on the SOMATOM Force.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...
The Issue: Suboptimal routing of the cable may result in increased wear over time....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (R)Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.