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. 2,881 recalls have been distributed to California in the last 12 months.
Showing 20001–20020 of 30,923 recalls
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Pads Recalled by Terumo...
The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090 Recalled by Signal...
The Issue: Potential for poly tip of the mallet to come off during use. Potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...
The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Sports Med Repicci II Tibial Components...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tubing Pack with Bioline Coating UDI code: 00607567208230 Part...
The Issue: A complaint was received on January 1, 2017 stating the pigtail on line 2 of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath Recalled by...
The Issue: One side of the MobiCath Bi-Directional Guiding Sheath pouch may not be sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit. Dialyzer Recalled by Baxter Healthcare Corporation...
The Issue: Firm has received reports of device operators failing to adhere to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule...
The Issue: When a user switches on MR1100 Receiver, even though the battery was fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital...
The Issue: Digital templates were created with the incorrect files.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UOC Femoral Driver Recalled by United Orthopedic Corporation Due to The...
The Issue: The locking lever pin component of the femoral driver may become deformed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...
The Issue: A damaged temperature sensor at the endoscope's tip can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...
The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.