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. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 24541–24560 of 52,535 recalls
Recalled Item: Pravastatin Sodium Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...
The Issue: Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biotin 10 mg/mL Injection Recalled by Auro Pharmacies Inc. DBA Central Drugs...
The Issue: Failed pH Specification: product does not meet pH label claim.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fayosim (levonorgestrel and ethinyl estradiol) tablets USP Recalled by Lupin...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha with software version VA30-mobile C-arm x-ray Material # Recalled...
The Issue: Continuous operation of the Cios Alpha at high tube outputs may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...
The Issue: The back cover of the light head was insufficiently assembled and could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...
The Issue: The back cover of the light head was insufficiently assembled and could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV1000 Clinical Platform Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Potential for an electrical short circuit leading to possible fire hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System 10 MM Recalled by Conmed Corporation...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Clinician Programmer (Touchscreen) Software version 2.00.29...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmer (Grand Prime) Software version 2.00.29 Recalled by...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump Recalled by Flowonix Medical Inc Due to The...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.