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. 1,043 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,043 in last 12 months

Showing 41761–41780 of 56,506 recalls

Medical DeviceJuly 1, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...

The Issue: A problem exists in MOSAIQ resulting in the incorrect field size being sent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Processor EPX 2500 High Definition Endoscopy Recalled by Fujifilm...

The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· BIOTRONIK, Inc.

Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...

The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Acetaminophen reagents Recalled by Siemens Healthcare...

The Issue: A change in the concentration of N-acetylcysteine (NAC) that may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic...

The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Scenaria Computed Tomography System Hitachi Medical Systems America...

The Issue: The firm discovered that the centrifugal force applied to the power supply...

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

Class II — Potential Health HazardOngoing
DrugJune 30, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...

The Issue: Crystallization; identified as calcium salt of Ketorolac

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2015· Mylan Pharmaceuticals Inc

Recalled Item: Capecitabine Tablets Recalled by Mylan Pharmaceuticals Inc Due to Failed...

The Issue: Failed Dissolution Specifications: low out-of-specification (OOS) results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...

The Issue: Crystallization; identified as calcium salt of Ketorolac

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2015· Michael Foods, Inc.

Recalled Item: Crystal Farms Simply Potatoes Shredded Hash Browns packaged as individual...

The Issue: Product may contain small slivers of shredded golf ball.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2015· Inn Foods Inc.

Recalled Item: IQF Italian Cut Green Beans (each tote 1350 lbs) lot Recalled by Inn Foods...

The Issue: Due to customer request a sample of IQF Italian Cut Green Beans was sent to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing