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. 1,074 recalls have been distributed to California in the last 12 months.
Showing 33481–33500 of 56,506 recalls
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Art-Line Surgery Pack-LF Recalled by Medline Industries, Inc. Due to...
The Issue: Multiple surgical packs were assembled with a non-sterile CHG disk labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Tray Recalled by Medline Industries, Inc. Due to Multiple surgical...
The Issue: Multiple surgical packs were assembled with a non-sterile CHG disk labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Insulation Pad Recalled by Medline Industries, Inc. Due to Complete...
The Issue: Complete delivery System (CDS) # CDS984746C was assembled using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscopy CDS Recalled by Medline Industries, Inc. Due to One...
The Issue: One manufacturing lot of a non-sterile pack was assembled with a non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER CDS Recalled by Medline Industries, Inc. Due to Multiple surgical...
The Issue: Multiple surgical packs were assembled with a non-sterile CHG applicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dolphin Inflation Device Recalled by Vascular Solutions, Inc. Due to The...
The Issue: The manufacturer of the DOLPHIN inflation device, Perouse Medical, has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...
The Issue: An unexpected transient mode switch behavior was detected by Medtronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...
The Issue: An extremely dusty computer can cause problems at system start, or rarely,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...
The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...
The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI . The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Bakery Peanut Butter Chocolate Chunk Cookies Recalled by Jimmy's Cookies...
The Issue: The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EasyCAL HbA1c Calibrator Recalled by Medica Corporation Due to Patient...
The Issue: Patient results determined using this calibrator lot might deviate up to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.