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. 2,654 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,654 in last 12 months

Showing 4568145700 of 56,506 recalls

FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Arriba! 16 oz. Chili Con Queso-Hot Recalled by Riba Foods Inc Due to...

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Salpica 8 oz. Ballpark Nacho Recalled by Riba Foods Inc Due to Undeclared Wheat

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Karlsburger Foods, Inc.

Recalled Item: InHarvest Garden Vegetable Seasoning Recalled by Karlsburger Foods, Inc. Due...

The Issue: Firm is recalling Garden Vegetable Seasoning due to an undeclared milk allergen.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 10, 2014· GE Inspection Technologies, LP

Recalled Item: GE Optional Laser Centering Device X-ray generator. Recalled by GE...

The Issue: GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...

The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· CSA Medical

Recalled Item: CSA Medical truFreeze System Recalled by CSA Medical Due to An increase in...

The Issue: An increase in complaint trending for a loss of audible sound associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· GE Inspection Technologies, LP

Recalled Item: GE Cabinet X-ray systems Recalled by GE Inspection Technologies, LP Due to...

The Issue: GE discovered these cabinet x-ray systems' potential failure to comply with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· Arrow International Inc

Recalled Item: Arrow Nerve Block Component Recalled by Arrow International Inc Due to Arrow...

The Issue: Arrow is recalling certain lots of the Continuous Nerve Block Component,...

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

Class II — Potential Health HazardOngoing
DrugNovember 7, 2014· Hospira Inc.

Recalled Item: Sterile powder Vancomycin Hydrochloride for Injection Recalled by Hospira...

The Issue: Correct Labeled Product Mispack: Product tray containing vials was...

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

Class III — Low RiskOngoing
Refund
FoodNovember 7, 2014· Marin Food Specialties Inc

Recalled Item: Whole Foods Organic Raw Almonds Imported from Spain USDA Organic Recalled by...

The Issue: Customer reported high levels of hydrogen cyanide in Raw Organic almonds...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Comfort 5+5 Pack w/110cm Tube & 17mm Cann. UPC# 3-89110-14147-7 Recalled by...

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: AC TenderLink 13/30 10 pcs Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Contact Detach Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Silhouette Paradigm 13mm Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: SureT G29 6mm Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Infusion Set Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Breas Medical AB

Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...

The Issue: Unintended treatment termination could result from a keypad malfunction in...

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

Class II — Potential Health HazardOngoing