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. 2,989 recalls have been distributed to California in the last 12 months.
Showing 13081–13100 of 30,923 recalls
Recalled Item: TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: Recalled by Smith &...
The Issue: Due to a potential for sterile barrier breach. A complaint was received that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dawson-Mueller Drainage Catheter Recalled by Cook Inc. Due to Specific lots...
The Issue: Specific lots of the Dawson-Mueller Drainage Catheter were not manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II 20mL Pump. Catalog No. 13827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 91827 The device is Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US Clinical 20mL Programmable Pump. Catalog No. 01827 The device Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 11827 The device is Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable 20mL Pump. Catalog No. 93827 The device Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II 40mL Pump. Catalog No. 16827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225...
The Issue: The manufacturer identified a risk that their products might fail to comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wave Prep Tubes (1710-03) and single use cups (17--00-24) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...
The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Tapered Guided Surgery Drill Recalled by Jjgc Industria E Comercio...
The Issue: The laser engraving of the product incorrectly identifies the 4.3 Tapered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...
The Issue: Potential for the expiration date on the outer label that was applied by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.