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. 2,680 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,680 in last 12 months

Showing 1024110260 of 50,223 recalls

DrugJanuary 12, 2023· Accord Healthcare, Inc.

Recalled Item: Allopurinol Tablets USP Recalled by Accord Healthcare, Inc. Due to Presence...

The Issue: Presence of Foreign Substance: Presence of a small piece of green plastic...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2023· Nephron Sc Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Nephron Sc Inc Due to CGMP...

The Issue: CGMP Deviations: potential for trace amounts of product carryover.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2023· Nephron Sc Inc

Recalled Item: Sterile Water for Injection Recalled by Nephron Sc Inc Due to CGMP...

The Issue: CGMP Deviations: potential for trace amounts of product carryover.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2023· Ortho Molecular Products, Inc.

Recalled Item: Fiber Powder Recalled by Ortho Molecular Products, Inc. Due to Raw material...

The Issue: Raw material tested positive for Cronobacter sakazakii.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2023· Amerisource Health Services LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications: This recall is being initiated in support...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2023· Consolidated Chemical, Inc

Recalled Item: Humatrix Microclysmic Gel Recalled by Consolidated Chemical, Inc Due to CGMP...

The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2023· Consolidated Chemical, Inc

Recalled Item: Techni-Care Chloroxylenold 3% Recalled by Consolidated Chemical, Inc Due to...

The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2023· THE ISH COMPANY

Recalled Item: ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) Recalled by THE ISH...

The Issue: undeclared soy proteins

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
DrugJanuary 6, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· MACLEODS PHARMA USA, INC

Recalled Item: Levofloxacin Tablets Recalled by MACLEODS PHARMA USA, INC Due to Mismatching...

The Issue: Mismatching of the embossing on the tablets (T7) with the embossing...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 5, 2023· S & MOHR AMERICA, S.A. DE C.V.

Recalled Item: abm Respiratory Care Standart Breating Circuit with Face Mask - Recalled by...

The Issue: Incorrect expiration date on product label. The manufacturing date was...

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

Class III — Low RiskOngoing