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. 1,217 recalls have been distributed to California in the last 12 months.
Showing 2801–2820 of 30,923 recalls
Recalled Item: Merlin.net Patient Care Network (PCN) Heart Failure Web Application (Model...
The Issue: Due to a data migration from on-premises server to the cloud environment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscissor Tip (Disposable) Recalled by Microline Surgical, Inc. Due to A...
The Issue: A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V.A.C. Ulta Therapy Unit & ULTDEV01 The 3M" Recalled by KCI USA, INC. Due to...
The Issue: Due to potential system error alarm and the inability to initiate therapy as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOA Medical Industries Behavioral Health Hospital bed side rails Recalled by...
The Issue: Red button used to engage side rails can break or become stuck making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CI Analyzer. Catalog Numbers: 10947347. Recalled by Siemens...
The Issue: Potential that the IMT Diluent volume remaining (% remaining) does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Breast Coil 3.0T 7ch Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva TX Interventional Coil 3.0T Recalled by Philips North America Llc...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 7ch 3.0T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 7ch 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Diagnostic Coil 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Diagnostic Coil 3.0T Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 16ch 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Interventional Coil 1.5T Recalled by Philips North America Llc Due...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Interventional Coil 3.0T Recalled by Philips North America Llc Due...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BYTE Aligner System BYTE All-Day Aligner System BYTE Recalled by Straight...
The Issue: Virtual-only clinical workflow utilized for dental aligners and impression...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 16ch 3.0T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST SENSE Breast Dx Coil Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Server Software Versions 11.1.4 through 11.1.6 Recalled by Securitas...
The Issue: Certain software versions will not notify end users of calls initiated by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.