BOULDER, Colo.--(BUSINESS WIRE)--Jan. 19, 2012--
On November 8, 2011, Covidien initiated a voluntary recall of certain
lots of its BIS™ Bilateral Sensors, due to a modification which
inadvertently reversed the reference and left eye electrode. This
modification could potentially cause a change in the performance of BIS
monitoring systems when these sensors are used, resulting in the
inaccurate calculation and presentation of processed EEG information for
Bispectral Index™ (BIS), Density Spectral Array (DSA), and Asymmetry
(ASYM) values.
To date, there have been no reports of patient injury related to the
recalled products.
The voluntary recall only affects lot numbers manufactured during a
specific period of time. Only BIS Bilateral Sensors from the 58 lot
numbers listed below are affected by this action.
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0528111A
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0624111A
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0727111A
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0811111A
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0824111A
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0926111A
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0603111A
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0625111A
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0727111B
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0812111A
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0824111B
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0927111A
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0604111A
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0627111A
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0728111A
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0813111A
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0825111A
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0930111A
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0606111A
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0701111A
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0728111B
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0814111A
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0825111B
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1001111A
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0607111A
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0707111A
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0729111A
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0820111A
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0826111A
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1003111A
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0608111A
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0712111A
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0729111B
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0821111A
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0826111B
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1004111A
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0609111A
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0713111A
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0801111A
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0822111A
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0921111A
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1005111A
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0615111A
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0725111A
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0808111A
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0822111B
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0923111A
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1006111A
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0620111A
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0726111A
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0809111A
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0823111A
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0923111B
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0621111A
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0726111B
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0810111A
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0823111B
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0924111A
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Customers were first notified about this issue by letter dated November
8, 2011. The Company has taken appropriate steps to address the issue,
and adequate supplies of unaffected replacement product are available.
Customers should review product in inventory and current use to identify
product from the affected lot codes and return affected lots to
Covidien. To return the affected product for replacement product,
contact Technical Services at 1-800-635-5267, option 3, then option 1,
and reference the Return Goods Authorization (RGA) Number in the recall
letter.
Healthcare professionals and customers may report adverse events or
quality problems experienced with the use of this product to the FDA's
MedWatch Adverse Event Reporting program either online, by regular mail,
fax or by phone.

Source: Covidien
Covidien
Rhonda Luniak, 303-406-8743
Vice President,
Communications
Respiratory & Monitoring Systems
rhonda.luniak@covidien.com
or
Bruce
Farmer, 508-452-4372
Vice President
Public Relations
bruce.farmer@covidien.com
or
Coleman
Lannum, CFA, 508-452-4343
Vice President
Investor Relations
cole.lannum@covidien.com
or
Todd
Carpenter, 508-452-4363
Director
Investor Relations
todd.carpenter@covidien.com