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SYRINGE RECALL

Syringe Recall Last Edited: Thursday, 06 Nov 2008, 6:06 AM PST Created: Thursday, 06 Nov 2008, 6:06 AM PST

NEWS RELEASE:

The U.S. Food and Drug Administration is notifying health care

professionals and patients that Tyco Healthcare Group LP (Covidien) is

recalling one lot of ReliOn sterile, single-use, disposable, hypodermic

syringes with permanently affixed hypodermic needles due to possible

mislabeling. The use of these syringes may lead to patients receiving an overdose of as much as 2.5 times the intended dose, which may lead to hypoglycemia, serious health consequences, and even death.

The recall applies to the following lot number and product information:

--Lot Number 813900

--ReliOn 1cc, 31-gauge, 100 units for use with U-100

insulin

Only ReliOn syringes from this lot number and labeled as 100 units for

use with U-100 insulin are the subject of the recall.

These syringes are distributed by Can-Am Care Corp and sold only by

Wal-Mart at Wal-Mart stores and Sam's Clubs under the ReliOn name.

Wal-Mart requests that all users of ReliOn 31-gauge, 1cc syringes return those labeled as 100 units for use with U-100 insulin from Lot Number 813900 to their local Wal-Mart store or Sam's Club pharmacy. Customers will be provided with replacement product.

The FDA urges patients and health care professionals to check their

syringe packaging carefully for syringes labeled as 100 units for use

with U-100 insulin from Lot Number 813900.

Consumers and health care professionals who suspect they have the

recalled product may also contact Covidien at 866-780-5436 or

www.relion.com/recall for more information.

ReliOn Insulin Syringes consist of a syringe barrel, a plunger rod, and

a hypodermic needle attached to the tip of the syringe.

During the packaging process for this lot, some syringes labeled for use

with U-40 insulin were mixed with syringes labeled for use with U-100

insulin, then all packaged individually and in boxes as 100 units for

use with U-100 insulin.

The manufacturer has distributed 4,710 boxes in the recalled lot, which

equals 471,000 individual syringes. Wal-Mart sold the syringes at

Wal-Mart stores and Sam's Clubs from Aug. 1, 2008, until Oct. 8, 2008.

Tyco Healthcare Group LP (Covidien) voluntarily recalled this lot of

syringes on Oct. 9, 2008, asking that any units of the affected product

be removed from inventory and placed in quarantine. Wal-Mart posted the recall announcement in Wal-Mart stores and Sam's Clubs, as well as on its Web site, and sent letters to more than 16,500 customers notifying them of the recall.

The manufacturer has received one adverse report related to a syringe

from this product lot.Health care professionals and consumers may report serious adverse events (side effects) or product quality problems with the use of this product to the FDA's MedWatch Adverse Event Reporting program eitheronline, by regular mail, fax or phone.

--Online: www.fda.gov/MedWatch/report.htm

--Regular Mail: use postage-paid FDA form 3500 available at:

www.fda.gov/MedWatch/getforms.htm and mail to

MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787

--Fax: (800) FDA-0178

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