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. 2,648 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,648 in last 12 months

Showing 3378133800 of 52,535 recalls

Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Halyard Health, Inc

Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...

The Issue: Drapes within the affected lots may include a manufacturing variation that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
DrugNovember 8, 2016· Care-Tech Laboratories, Inc.

Recalled Item: Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or...

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

Class III — Low RiskOngoing
Refund
FoodNovember 8, 2016· Chaos and Pain

Recalled Item: CANNIBAL FEROX AMPED Recalled by Chaos and Pain Due to Product was analyzed...

The Issue: Product was analyzed and found to contain 1,3- dimethylbutylamine which was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2016· Meridian Bioscience Inc

Recalled Item: PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due...

The Issue: Internal testing has demonstrated that the indicated kit lots produce false...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Performance-LOAD Ambulance Cot Fastener Stretcher Recalled by Stryker...

The Issue: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
DrugNovember 7, 2016· Pfizer Inc.

Recalled Item: LEVOXYL(R) (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...

The Issue: Superpotent

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 7, 2016· Helena Laboratories, Inc.

Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...

The Issue: Due to a customer experiencing complaints on bone fraction of assay not...

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

Class III — Low RiskOngoing
Medical DeviceNovember 7, 2016· Tosoh Bioscience, Inc.

Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...

The Issue: The device defect associated with this recall may result in HbA1c values...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Bayer Healthcare

Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...

The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Alteon Neck Preserving Stem Recalled by Exactech, Inc. Due to Products were...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Novation Cemented Plus Femoral Stem Recalled by Exactech, Inc. Due to...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing