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. 2,940 recalls have been distributed to California in the last 12 months.
Showing 16781–16800 of 30,923 recalls
Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...
The Issue: Label was incorrect. The label states that the volume of the retrieval bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...
The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tri-Flo Subglottic Suction System Recalled by Vyaire Medical Due to...
The Issue: Vyaire Medical has discovered potential patient safety risk with associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: Through investigation, it was determined that H12LP Trocars in scope of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number:...
The Issue: Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Shepherd' s Hook - Greenberg Recalled by Nico Corp. Due to Mislabeling
The Issue: Mislabeled hook pouch included a transport/storage label rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a...
The Issue: There is a potential risk associated with the PEEK tip of the J-Plasma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPAP Mask Cushion Recalled by Compass Health Brands (Corporate Office) Due...
The Issue: A May 2015 design change in the cushion seal replacement part and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Bolt Recalled by Zimmer Biomet, Inc. Due to Product was...
The Issue: Product was manufactured from the incorrect material, which shows a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slit Knife 2.6mm 45degree Bevel Up Recalled by Beaver Visitec Due to Mislabeling
The Issue: Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI system Product Usage: Hitachi MR system is Recalled by...
The Issue: The stainless steel belt which runs the length of the table underneath the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brush Recalled by Medline Industries Inc Due to There is...
The Issue: There is potential risk of brush detachment during cleaning. If brush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 1 36" 90 cm Undyed GS-21 Recalled by...
The Issue: Potential proplylene glycol contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by Maquet SAS Due to Certain VOLISTA...
The Issue: Certain VOLISTA StandOP Surgical Lights have been identified as having a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111 Recalled by...
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY BCS OXINIUM Knee Femoral Components Recalled by Smith & Nephew, Inc....
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Journey BCS Knee CoCr Femoral Components Recalled by Smith & Nephew, Inc....
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Biosystems HistoCore SPECTRA ST Recalled by Leica Microsystems, Inc....
The Issue: These devices have an incorrect specification against safety standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-SPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoSPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.