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. 2,636 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,636 in last 12 months

Showing 3534135360 of 52,535 recalls

Medical DeviceJuly 1, 2016· Carefusion 2200 Inc

Recalled Item: DIAMOND-FLEX CIRCULAR RETRACTOR Recalled by Carefusion 2200 Inc Due to BD,...

The Issue: BD, formerly CareFusion, has identified a potential risk associated with a...

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

Class I — Serious Health HazardOngoing
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Actavis Inc

Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...

The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2016· General Mills, Inc

Recalled Item: Case: Beyond Meat Vegetarian Indian Curry with Beyond Chicken Recalled by...

The Issue: General Mills today announced a voluntary recall of a limited quantity of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Gmbh

Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...

The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...

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

Class II — Potential Health HazardOngoing
DrugJune 29, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection Recalled by...

The Issue: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: ArjoHuntleigh Sara Combilizer Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....

The Issue: ArjoHuntleigh has concluded that a device tipping hazard may occur on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· C.R. Bard, Inc.

Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem

The Issue: Labeling problem

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

Class III — Low RiskOngoing
DrugJune 28, 2016· Golden State Medical Supply Inc.

Recalled Item: DULOXETINE Delayed-Release Capsules Recalled by Golden State Medical Supply...

The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 28, 2016· Medtronic Xomed, Inc.

Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to Wire in...

The Issue: Wire in tubing can become exposed, posing potential harm to the intubated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing