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. 2,727 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,727 in last 12 months

Showing 1750117520 of 52,535 recalls

Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...

The Issue: Subpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Methylprednisolone Tablets USP Recalled by Jubilant Cadista Pharmaceuticals,...

The Issue: Labeling: Illegible label: Customer complaint received of mis-alignment...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodFebruary 19, 2021· Seafood Imports Distributors Inc.

Recalled Item: Java Frozen Tuna Steaks - 10 oz. Net Wt. 10 Recalled by Seafood Imports...

The Issue: FDA Sample found Salmonella in one lot of 10 oz. frozen tuna steaks.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 18, 2021· Ferrara Candy Company

Recalled Item: Ferrara Candy Company assorted candy Heart Box Recalled by Ferrara Candy...

The Issue: Undeclared ingredients on retail packaging, including but not limited to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 18, 2021· TELEFLEX MEDICAL INC

Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...

The Issue: Teleflex is voluntarily recalling the products above due to customers...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Sunstar Americas, Inc.

Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...

The Issue: The product may be contaminated with Burkholderia cepacia

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...

The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01...

The Issue: Crystallization: customer complaints for crystallization in finished product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 18, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01...

The Issue: Crystallization: customer complaints for crystallization in finished product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 17, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Imatinib Mesylate Tablets 100mg Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2021· Edge Pharma, LLC

Recalled Item: Methacholine Challenge 5-Syringe Test Kits Recalled by Edge Pharma, LLC Due...

The Issue: Temperature Abuse; labeled with the incorrect room temperature (15-25 ¿C)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund