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. 2,819 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,819 in last 12 months

Showing 3356133580 of 56,506 recalls

Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Back Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2017· Stryker Medical Division of Stryker Corporation

Recalled Item: Medi-Therm Hyper/Hypothermia System Recalled by Stryker Medical Division of...

The Issue: The water may reheat too quickly if the unit is in "Automatic" mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2017· Teleflex Medical

Recalled Item: Arrow EZ-IO Needle Set 45 mm 15 ga Recalled by Teleflex Medical Due to Some...

The Issue: Some of the individual unit packaging (pouches) may be missing the lot...

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

Class III — Low RiskOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GP321R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software error - As a result of a software fault in Artis zee systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Bard Peripheral Vascular Inc

Recalled Item: MR GHIATAS Beaded Breast Localization Wire Recalled by Bard Peripheral...

The Issue: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GP161R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GE426R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
DrugMarch 28, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Taro Pharmaceuticals...

The Issue: Failed Content Uniformity Specifications; out-of-specification (OOS) results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2017· Teva Pharmaceuticals USA

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 28, 2017· Envy Me

Recalled Item: LaBri's Body Health Atomic Recalled by Envy Me Due to Undeclared Sibutramine

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2017· Gary Wood

Recalled Item: hCG Body Shaper Recalled by Gary Wood Due to Marketed without an Approved...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis has found the product to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 27, 2017· Alcon Research, Ltd.

Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...

The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2017· Mentor Texas, LP.

Recalled Item: Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast...

The Issue: Missing Dome Pack accessory.

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

Class II — Potential Health HazardOngoing
FoodMarch 27, 2017· The French's Food Company, LLC SUBS Reckitt Benckiser

Recalled Item: French's Crispy Jalapenos Net Wt. 5 oz. (141.7g) Recalled by The French's...

The Issue: Product may contain foreign objects: rocks and metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing