Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,466 recalls have been distributed to Wyoming in the last 12 months.
Showing 18101–18120 of 27,462 recalls
Recalled Item: Thoracentesis/ Paracentesis Kit 10/CS Recalled by Carefusion 2200 Inc Due to...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5 Recalled by Carefusion 2200...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Internal Hex Healing Abutment Recalled by Ace Surgical Supply Co.,...
The Issue: Incorrect device was packaged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS-636 Recalled by Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc....
The Issue: Incorrect priming volume printed on the device package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software updates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090 Recalled by Signal...
The Issue: Potential for poly tip of the mallet to come off during use. Potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartTools Knee System Orthopedic Stereotaxic Instrument Recalled by...
The Issue: There has been an increase in the number of complaints regarding bent or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint - 3R Recalled by Siemens Medical Solutions USA Inc....
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...
The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Pads Recalled by Terumo...
The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.