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. 2,696 recalls have been distributed to Nevada in the last 12 months.
Showing 6221–6240 of 50,223 recalls
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to The Alinity m...
The Issue: The Alinity m System camera detects whether tubes are "capped." If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Surgical Tape Recalled by 3M Company - Health Care Business Due...
The Issue: Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr¿ger Perseus A500 Anesthesia Workstation Recalled by Draeger Medical, Inc....
The Issue: Unexpected shutdown while operating on battery power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weiner Boner Honey Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flower Power Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pink Pussycat Honey Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spanish Fly 22K capsules Recalled by Pyramids Wholesale Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Samurai-X Honey 6800 Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALPHASTRIP MALE PERFORMANCE ENHANCER Recalled by Pyramids Wholesale Inc. Due...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HONEY MANUKA BUNNY LOVE Recalled by Pyramids Wholesale Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SILVERBACK XXX POWER MALE ENHANCEMENT Recalled by Pyramids Wholesale Inc....
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The GOAT SUBLINGUAL STRIP Recalled by Pyramids Wholesale Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: libigrow RED DRAGON+ Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.