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. 1,132 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,132 in last 12 months

Showing 1101–1120 of 50,223 recalls

FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Good & Gather Mozzarella & Parmesan shredded cheese blend Recalled by Great...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Mozzarella and provolone shredded cheese blend (containing low-moisture...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Low-moisture part-skim mozzarella shredded cheese Recalled by Great Lakes...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2025· Great Lakes Cheese Co Inc

Recalled Item: Happy Farms by Aldi Italian Style shredded cheese blend (containing Recalled...

The Issue: Potential metal fragments from supplier raw material (downstream recall)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2025· Cerenovus Inc

Recalled Item: CEREPAK Detachable Coil System - Name/ 2MM X 2.5 CM/FCX100202 Recalled by...

The Issue: Detachable coils system may fail to detach, which could result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 2, 2025· ICU Medical, Inc.

Recalled Item: IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave Recalled by...

The Issue: IV Gravity burette administration set burette component is missing an...

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

Class I — Serious Health HazardOngoing
DrugOctober 1, 2025· Church & Dwight Co., Inc.

Recalled Item: ZICAM" MEDICATED FRUIT DROPS ELDERBERRY FLAVOR Recalled by Church & Dwight...

The Issue: Labeling: Label Mix-up: The product in the bottle contains elderberry and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2025· Aspiro Pharma Limited

Recalled Item: Ketorolac Tromethamine Injection Recalled by Aspiro Pharma Limited Due to...

The Issue: Presence of Particulate Matter: Particulate matter identified as glass

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline RenewalLigasure Blunt Tip Sealer/Divider Recalled by Medline...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: ProxiDiagnost N90 Recalled by Philips Medical Systems DMC GmbH Due to...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: CombiDiagnost R90 Recalled by Philips Medical Systems DMC GmbH Due to...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: Radiography 7300 C Recalled by Philips Medical Systems DMC GmbH Due to...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
FoodOctober 1, 2025· DEMERS FOOD GROUP LLC

Recalled Item: Scott & Jon s Shrimp Scampi with Linguine Recalled by DEMERS FOOD GROUP LLC...

The Issue: Contains Linguine manufactured by Nate's Fine Foods LLC recalled for...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal LigaSure Blunt Tip Sealer/Divider Recalled by Medline...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal Ligasure Impact Sealer/Divider NanoCoated Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Philips Medical Systems DMC GmbH

Recalled Item: DigitalDiagnost C90 (1) High Performance Recalled by Philips Medical Systems...

The Issue: Philips has identified that some ceiling suspension telescopic carriages...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated Recalled by...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2025· Medline Industries, LP

Recalled Item: Medline Renewal LigaSure Exact Recalled by Medline Industries, LP Due to...

The Issue: Medline Renewal has determined that certain areas on the device have the...

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

Class II — Potential Health HazardOngoing