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. 1,025 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,025 in last 12 months

Showing 22821–22840 of 50,223 recalls

Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Sys2.7 Recalled by Zimmer GmbH Due to An investigation identified that...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS high Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS high Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Osteofresh arthrodesis drill Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Test PROCYP (TESTOSTERONE CYPIONATE 200MG/ML TESTOSTERONE PROPIONATE...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML Recalled by Customceutical...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5 Recalled by...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Trimix HIGH (Papaverine HCl 30 mg/mL Phentolamine Mesylate 2 mg/mL Recalled...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 Recalled by...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· American Health Packaging

Recalled Item: GlipiZIDE Extended-release Tablets Recalled by American Health Packaging Due...

The Issue: Failed Dissolution Specifications: dissolution failure at time zero of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Lipoplex (METHIONINE 25 MG/ML INOSITOL 50 MG/ML CHOLINE CHLORIDE 50 Recalled...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: TriMix MEDIUM (Papaverine HCL 21 mg/mL Phentolamine Mesylate 0.7 mg/mL...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2019· Customceutical Compounding

Recalled Item: Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5 Recalled by...

The Issue: Lack of assurance of sterility for injectables and solutions intended to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2019· Brian P. Richardson

Recalled Item: Kopi Jantan Tradisional Natural Herbs Coffee Recalled by Brian P. Richardson...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 5, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Potential loose cable connections on the reagent cooler, which could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2019· Advanced Bionics, LLC

Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...

The Issue: The manufacturer received complaints that customers were attempting to...

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

Class III — Low RiskOngoing