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. 3,068 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,068 in last 12 months

Showing 14411460 of 56,506 recalls

Medical DeviceSeptember 17, 2025· Percussionaire Corporation

Recalled Item: Phasitron 5 Recalled by Percussionaire Corporation Due to IFU update;...

The Issue: IFU update; in-line valve, with pressure relief seal may leak when used with...

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

Class I — Serious Health HazardOngoing
FoodSeptember 16, 2025· Sprout Organics Inc.

Recalled Item: 6+ Months SPROUT ORGANICS Made With Organic Sweet Potato Recalled by Sprout...

The Issue: Potential contamination with heavy metal (Lead).

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 16, 2025· Gansu Zhaofeng Agricultural Development Co., Ltd.

Recalled Item: G&L Food Dried Bean Curd Net WT 17.6 OZ (500G) INGREDIENTS: Soybean Recalled...

The Issue: Undeclared allergen (wheat).

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

Class III — Low RiskOngoing
Refund
DrugSeptember 16, 2025· IntegraDose Compounding Services LLC

Recalled Item: Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use...

The Issue: Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 16, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent: During long term stability testing of Levothyroxine Sodium...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 16, 2025· Medtronic Sofamor Danek USA Inc

Recalled Item: Catalyft PL & PL40 Expandable Interbody System labeled as follows Recalled...

The Issue: Expandable interbody system cage may loose height or collapse (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...

The Issue: A software anomaly, under specific conditions when large rotational...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Spacelabs Healthcare, Ltd.

Recalled Item: Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number:...

The Issue: Due to two distinct issues: 1. During patient admission, patient demographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Surgical Planner Recalled by Surgical Theater Inc Due to A software anomaly,...

The Issue: A software anomaly, under specific conditions when large rotational...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: SuRgical Planner (SRP) Recalled by Surgical Theater Inc Due to A software...

The Issue: A software anomaly, under specific conditions when large rotational...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP)...

The Issue: A software anomaly, under specific conditions when large rotational...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: SpineAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...

The Issue: A software anomaly, under specific conditions when large rotational...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Surgical Navigation Advanced Platform (SNAP) Recalled by Surgical Theater...

The Issue: A software anomaly, under specific conditions when large rotational...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Surgical Theater Inc

Recalled Item: Surgical Navigation Advanced Platform Patient Engagement (PE SNAP) Recalled...

The Issue: A software anomaly, under specific conditions when large rotational...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2025· Abiomed, Inc.

Recalled Item: Automated Impella Controller (AIC) labeled as the following with...

The Issue: Potential for Automated Impella Controller (AIC) purge pressure issues due...

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

Class I — Serious Health HazardOngoing
DrugSeptember 15, 2025· Graviti Pharmaceuticals Private Limited

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (XL) Recalled by...

The Issue: Failed Tablet/Capsule Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2025· Amerisource Health Services LLC

Recalled Item: Carbamazepine Extended-Release Tablets Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 15, 2025· Alcon Research LLC

Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2025· FUJIFILM Healthcare Americas Corporation

Recalled Item: FDR Visionary Suite Recalled by FUJIFILM Healthcare Americas Corporation Due...

The Issue: It was found that the shaft for mounting the X-ray tube unit on the support...

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

Class II — Potential Health HazardOngoing
FoodSeptember 12, 2025· MARS FOODS US

Recalled Item: Ben's Original Ready Rice Long Grain & Wild Recalled by MARS FOODS US Due to...

The Issue: Possible presence of stones in product

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

Class II — Potential Health HazardOngoing
Refund