Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 3,000 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,000 in last 12 months

Showing 1122111240 of 56,506 recalls

FoodJanuary 10, 2023· DAISO CALIFORNIA WAREHOUSE

Recalled Item: Harvest Sesame 94g units Recalled by DAISO CALIFORNIA WAREHOUSE Due to...

The Issue: Product contains soy and sesame that are not listed on the ingredient label.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 10, 2023· DAISO CALIFORNIA WAREHOUSE

Recalled Item: TOHATO Bitter Caramel Corn 77g units Recalled by DAISO CALIFORNIA WAREHOUSE...

The Issue: Product contains almonds that are not listed on the ingredient label.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 10, 2023· DAISO CALIFORNIA WAREHOUSE

Recalled Item: Harvest Biscuits 4Kinds of Nuts 94g units Recalled by DAISO CALIFORNIA...

The Issue: Product contains soy and peanuts that are not listed on the ingredient label.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 10, 2023· DAISO CALIFORNIA WAREHOUSE

Recalled Item: Tohato 5packs of Caramel Corn 23g units Recalled by DAISO CALIFORNIA...

The Issue: Almond listed on the ingredient label but is not in Contains statement.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2023· DAISO CALIFORNIA WAREHOUSE

Recalled Item: TOHATO Caramel Corn - 80g units - pieces TOHATO Recalled by DAISO CALIFORNIA...

The Issue: Product contains almonds that are not listed on the ingredient label.

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

Class I — Serious 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
DrugJanuary 4, 2023· Intersect ENT, Inc.

Recalled Item: SINUVA (mometasone furoate) sinus implant Recalled by Intersect ENT, Inc....

The Issue: Failed Dissolution Specification; product did not meet the average 24-hour...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 4, 2023· Wishbone Medical, Inc.

Recalled Item: WishBone Medical Smart Correction Dual Joint Express Struts Recalled by...

The Issue: Firm identified that user may be unable to adjust the length of the Smart...

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

Class II — Potential Health HazardOngoing