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. 2,690 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,690 in last 12 months

Showing 2442124440 of 29,093 recalls

Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Becton Dickinson & Company

Recalled Item: BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection Recalled...

The Issue: BD received some reports of open seals found on the BD Posiflush SF Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Abbott Laboratories

Recalled Item: ICT Serum Calibrator . For use in the calibration Recalled by Abbott...

The Issue: ICT Serum Calibrator may generate lower than expected Potassium Quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 4.5 mm Malleolar Screw Sterile zimmer Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw Fully Threaded Sterile zimmer Recalled by Zimmer,...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw 32 mm Thread Length Sterile zimmer Recalled by...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw 16 mm Thread Length Sterile zimmer Recalled by...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw Fully Threaded Sterile zimmer Recalled by Zimmer,...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 4.0 mm Cancellous Screw Recalled by Zimmer, Inc. Due to Zimmer is recalling...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· GF Health Products, Inc./d.b.a.Basic American Metal Products

Recalled Item: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...

The Issue: The bed head deck may fail to elevate as expected during normal operation....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...

The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· BD Biosciences, Systems & Reagents

Recalled Item: BD Multi Check CD4 Low Control Catalog No. 340916 is Recalled by BD...

The Issue: The outer box label contains the incorrect distribution date: Box states...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Diagnostica Stago, Inc.

Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....

The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Cook Inc.

Recalled Item: CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a...

The Issue: This remedial action is the result of six product complaints associated with...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing