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. 2,696 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,696 in last 12 months

Showing 4056140580 of 56,506 recalls

DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Dexpanthenol Injection Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Cyanocobalamin Buffered Injectable 3mg/mL Recalled by Downing Labs, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Chromium Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2015· Utah Medical Products, Inc

Recalled Item: Myelo-Nate CSF Sampling Kit Recalled by Utah Medical Products, Inc Due to...

The Issue: Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2015· Arrow International Inc

Recalled Item: ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit...

The Issue: Possibility that the catheter peel-away component hub tabs may prematurely...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2015· Elekta, Inc.

Recalled Item: Monaco - Radiation Treatment Planning used to make treatment plans Recalled...

The Issue: Unintended update of Dose and MU and Incorrect Assignment of Bolus.

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

Class II — Potential Health HazardOngoing
FoodOctober 15, 2015· S. Martinelli & Co

Recalled Item: Martinelli's Sparkling Northwest Blend Cider Recalled by S. Martinelli & Co...

The Issue: Potential for glass fragments in 8.4 oz. bottles of four varieties of...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 15, 2015· S. Martinelli & Co

Recalled Item: Martinelli's Sparkling White Grape Recalled by S. Martinelli & Co Due to...

The Issue: Potential for glass fragments in 8.4 oz. bottles of four varieties of...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 15, 2015· S. Martinelli & Co

Recalled Item: Martinelli's Gold Medal Sparkling Cider Recalled by S. Martinelli & Co Due...

The Issue: Potential for glass fragments in 8.4 oz. bottles of four varieties of...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 15, 2015· S. Martinelli & Co

Recalled Item: Martinelli's Sparkling Red Grape Recalled by S. Martinelli & Co Due to...

The Issue: Potential for glass fragments in 8.4 oz. bottles of four varieties of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2015· Euro Diagnostica AB

Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...

The Issue: Complaint investigation concluded that although product quality requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2015· Merge Healthcare, Inc.

Recalled Item: DR Systems Unity PACS software Recalled by Merge Healthcare, Inc. Due to The...

The Issue: The software fails to associate to the correct MG image if there are two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· DeRoyal Industries Inc

Recalled Item: HYDRO-TEMP(R) Neonatal Temperature Skin Sensor Recalled by DeRoyal...

The Issue: DeRoyal manufactured four lots of HNICU-32, Hydro-Temp(R) Neonatal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...

The Issue: The following MRx software issue has been identified: MRx model M3535A with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Teleflex Medical

Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...

The Issue: The defective component can cause gas leakage through the device. This can...

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

Class II — Potential Health HazardOngoing