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. 2,722 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,722 in last 12 months

Showing 19211940 of 28,334 recalls

Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 Recalled by Ethicon Endo Surgery,...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2025· GE Medical Systems, LLC

Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...

The Issue: The battery for certain ultrasound systems can potentially develop an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2025· GE Medical Systems, LLC

Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...

The Issue: The battery for certain ultrasound systems can potentially develop an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen smart insulin pen Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pens may have been incorrectly assembled therefore users could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Medtronic Neuromodulation

Recalled Item: Stimulation RC Clinician Programmer Application Recalled by Medtronic...

The Issue: There is a software issue that can permanently disable communication with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) NAIL PACK Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) ED CRASH Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing