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. 2,674 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,674 in last 12 months

Showing 2848128500 of 29,093 recalls

Medical DeviceMay 21, 2012· Stryker Endoscopy

Recalled Item: Formula Shaver Handpiece (with buttons) Recalled by Stryker Endoscopy Due to...

The Issue: Stryker Endoscopy determined that there may not have been adequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker Rose Bed Model (FL14E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: GoBed+ . Model FL20E Beds are intended for medical purposes Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker MA204 Bed Model (FL25E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 1 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 4 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 3 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 10 Packaging: The product was packaged within Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 6 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 5 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· Boston Scientific Corporation

Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 27mm UPN Outer Box:...

The Issue: Difficulty in extending snare loop from the catheter

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

Class II — Potential Health HazardOngoing