Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,786 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,786 in last 12 months

Showing 4026140280 of 50,223 recalls

FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2014· Bleating Heart Cheese LLC

Recalled Item: Bleating Heart Cheese Recalled by Bleating Heart Cheese LLC Due to Potential...

The Issue: FDA samples found the presence of Listeria Monocytogenes in three varieties...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: CoCr Femoral Head - A modular head component is used Recalled by Zimmer Gmbh...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Metasul Femoral Head - indicated for total hip arthroplasty for Recalled by...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Metasul Femoral Head - A modular head component is used Recalled by Zimmer...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: CoCr Femoral Head - indicated for hip arthroplasty for noncemented Recalled...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Recalled by...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker...

The Issue: Potential for implant damage, implant cracking off/breaking intra-operatively.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...

The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Aesculap, Inc.

Recalled Item: Miethke Shunt System accessories Product Usage: - The Miethke Shunt Recalled...

The Issue: Some Miethke Shunt System accessories may have an incorrect MR safety symbol...

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

Class II — Potential Health HazardOngoing