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. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2566125680 of 30,923 recalls

Medical DeviceSeptember 8, 2014· Invivo Corporation

Recalled Item: Philips Expression MR200 MRI Patient Monitoring System Model 866120 Recalled...

The Issue: During production, excess metal (aluminum) debris was found stuck to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Teleflex Medical

Recalled Item: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...

The Issue: The pediatric breathing circuits can crack prior to and during use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 8, 2014· Xoran Technologies, LLC

Recalled Item: Xoran MiniCAT X-ray imaging device Recalled by Xoran Technologies, LLC Due...

The Issue: Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: Manual bunnell cranial drills are bone cutting and drilling instruments...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2014· Invivo Corporation

Recalled Item: Philips Expression MR200 MRI Patient Monitoring System Recalled by Invivo...

The Issue: Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has become aware of a potential safety issue involving missing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2014· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: The software issue described was corrected in the modification to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· GE Healthcare, LLC

Recalled Item: Discovery IGS 740 Indicated for use for patients from newborn Recalled by GE...

The Issue: Loss of imaging - affected devices may experience a loss of real-time...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· GE Healthcare, LLC

Recalled Item: Innova 4100IQ Indicated for use in generating fluoroscopic images of...

The Issue: Loss of imaging - affected devices may experience a loss of real-time...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· Teleflex Medical

Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...

The Issue: Misbranding: Although the product labeling identifies the catheters as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· GE Healthcare, LLC

Recalled Item: Innova IGS 540 Indicated for use for patients from newborn Recalled by GE...

The Issue: Loss of imaging - affected devices may experience a loss of real-time...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· DePuy Orthopaedics, Inc.

Recalled Item: RECLAIM Distal Reamer Extension Non Sterile Intended as Recalled by DePuy...

The Issue: Specific lots are being recalled due to the potential for the tabs to break,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Synthes, Inc.

Recalled Item: DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level Recalled by...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Ysio Max system The Ysio Max is a radiographic system used in...

The Issue: Two malfunctions posing potential risk to patients were identified with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing