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. 2,836 recalls have been distributed to California in the last 12 months.
Showing 30701–30720 of 30,923 recalls
Recalled Item: BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product affected by this notice is sold under the Recalled by RAYSEARCH...
The Issue: This field notice concerns two behaviors of the SharePlan (Multiple Fraction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source Recalled by...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare reported a...
The Issue: GE Healthcare reported a potential safety issue due to temporary loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM Central Station Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a....
The Issue: There is a software anomaly with the DPM Central Monitoring System where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Catalog (part number 20-0020) utilized with the Electric and...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cutting Bur Chart (part number 20-0019) utilized with the Electric Recalled...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00...
The Issue: Braemar Inc., became aware of a battery related incident that occurred with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Recalled by...
The Issue: In Online Entry (OEx) there are two scenarios where a Test result from one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IO FiX X-Post Reamer Recalled by Extremity Medical LLC Due to Product Event...
The Issue: Product Event Reports revealed a broken reamer experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IO Fix IntraOsseous Fixation System Recalled by Extremity Medical LLC Due to...
The Issue: Product Event Reports revealed that lag screw passes through washer (e.g....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Recalled by GE...
The Issue: GE Healthcare conducted a recall involving 2 events affecting the GE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 Neck Taper 00789504001 VerSys Femoral Head Provisional 40mm -3.5...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.