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. 2,631 recalls have been distributed to Nevada in the last 12 months.
Showing 14421–14440 of 28,334 recalls
Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...
The Issue: There is a potential for a loss of package integrity that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...
The Issue: There is a potential for a loss of package integrity that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...
The Issue: There is a potential for a loss of package integrity that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Needle Recalled by Terumo Medical Corporation Due to There is a...
The Issue: There is a potential for a loss of package integrity that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Needle Recalled by Terumo Medical Corporation Due to There is a...
The Issue: There is a potential for a loss of package integrity that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...
The Issue: There is a potential for a loss of package integrity that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Sur-vet Needle Recalled by Terumo Medical Corporation Due to There is...
The Issue: There is a potential for a loss of package integrity that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...
The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled...
The Issue: Frayed pieces of the mounting card being inside the primary packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medica Wash1-Wash solution used prior to Lipase assay on the Recalled by...
The Issue: Wash1 solution is ineffective in cleaning dispensing probe of TRIG and LDL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ PCV Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Locking Femoral Impactor Recalled by Encore Medical, Lp Due to The...
The Issue: The firm has received reports/complaints concerning the breakage of the tips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.