Reported Apr 1, 2015 · Terminated
Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067.…
Philips Medical Systems, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Medical Systems, Inc. · 3000 Minuteman Rd · Andover, MA · 01810-1032
Is this the product you have?
- Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS
- Part Number9065 and 9067. These rechargeable batteries are used to
- supply power to the following productsWireless ECG Module used with the Precess MRI compatible Patient Monitoring System, Wireless SpO2 Module used with the Precess MRI Compatible Patient Monitoring System, Philips Basic Triggering Set, Philips Monitoring Sensor Set, Philips Battery Set
- Lot codes and dates
- Batteries with date codes 2808 or earlier.
- Amount recalled
- 79
Where it was sold
Why it was recalled
VCG battery ignited in a VCG unit when recharging.
This product could cause temporary or reversible health problems — stop using it.
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