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. 2,583 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,583 in last 12 months

Showing 5034150360 of 52,535 recalls

Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT 3D 60 Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management Recalled by...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Acne Astringent Toner Pads (salicylic acid 2% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Severe Maximum Strength Acne Pore Cleanser (benzoyl peroxide 5%...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Original Strength Terminator (benzoyl peroxide 5% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 24 Hour Clearing System containing 1-count 4 fl oz Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Oil-Free Acne Cleanser (benzoyl peroxide 2.5% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 24 Hour Severe Acne Clearing System containing 1-count 4 Recalled...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Acne Pore Cleanser (benzoyl peroxide 2.5% w/v) Recalled by Valeant...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 3-in-1 Acne Night Repair Foam (retinol + salicylic acid 1.5% w/v)...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
FoodOctober 15, 2012· Hines Nut Co

Recalled Item: The HINES package is a cello/poly laminated bag Recalled by Hines Nut Co Due...

The Issue: Hines Nut Company Inc. recalled its SALTED JUMBO VIRGINIA IN-SHELL PEANUTS....

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 15, 2012· Ossur Americas, Inc.

Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...

The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Toshiba American Medical Systems Inc

Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...

The Issue: It was found that there is a problem with the LCD monitor used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· GE Healthcare, LLC

Recalled Item: Giraffe and Panda Bag and Mask Resuscitation System The T-piece Recalled by...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 15, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The Recalled...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing