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. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2526125280 of 56,506 recalls

DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: fentaNYL 1000 mcg/100 mL Injectable Solution Fentanyl 0.9% Sodium Chloride...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Morphine Sulfate 30 mg/30 mL (1 mg/mL) Injectable Solution Morphine Recalled...

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
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Dry Eye Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Dr. Berne's MSM DROPS 15% Solution Recalled by MSM Nutraceuticals, LLC Due...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· Akorn Inc

Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...

The Issue: Sub Potent Drug: OOS results observed for the Hydrocortisone assay during...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: 15% MSM Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Red Eye Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2019· Beaver Visitec

Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling

The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL Recalled by...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Elekta Limited

Recalled Item: Elekta Unity Recalled by Elekta Limited Due to Users need to be aware when...

The Issue: Users need to be aware when using these protocols for daily on line plan...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM)...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...

The Issue: One of the software algorithms used to detect sample dispense errors was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Brainlab AG

Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...

The Issue: There is a potential for an incorrect dose distribution calculation by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Randox Laboratories Ltd.

Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Customers...

The Issue: Customers may observe a decrease in recovered concentration with regards to...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2019· Teva Pharmaceuticals USA

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Teva...

The Issue: Subpotent Drug.

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

Class III — Low RiskOngoing
Refund
FoodMarch 10, 2019· Horizon Food Group

Recalled Item: Ne-Mo's Red Velvet Cake Square with Cream Cheese Icing Recalled by Horizon...

The Issue: Firm received a complaint of a bird foot found in the baked product.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2019· Horizon Food Group

Recalled Item: Ne-Mo's Chocolate Cake Square with Cream Cheese Icing Recalled by Horizon...

The Issue: Firm received a complaint of a bird foot found in the baked product.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2019· Horizon Food Group

Recalled Item: Ne-Mo's Birthday Cake Square with Buttercream Icing Recalled by Horizon Food...

The Issue: Firm received a complaint of a bird foot found in the baked product.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2019· Ardo N.V.

Recalled Item: Trader Joe s Fire Roasted Vegetables With Balsamic Butter Sauce Recalled by...

The Issue: Product label lists butter as an ingredient but does not declare milk.

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

Class II — Potential Health HazardOngoing
Refund