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February 06, 2012
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Drug Litigation News

 

Boca Medical Products Issues Recall of Insulin Syringe Product

 Boca Medical Products, Inc., of Coral Springs, Florida is initiating a recall of 3984 boxes of Ultilet Insulin Syringe 30g 1/2cc product lot number 5GEXI as displayed on the inner case.  The product is being recalled because of possible bacterial presence of Bacillus Cereus and Staphylococcus Intermedius.  This present a risk of local infection due to soft tissue injection with a contaminated syringe as well a risk of introduction of contaminating organism into previously sterile vial.  The introduced contamination may degrade the insulin, which could lead to problems maintaining insulin levels.  Boca Medical continues to evaluate possible risks.

Consumers who have Ultilet Syringe Insulin product lot 5GEXI, should stop usage and return the specific product.  Wholesalers should stop retail and return the product lot.  Send the product to Boca Medical Products Inc, 3550 NW 126 th Ave, Corals Springs, FL 33065.  Attention: Recall Contact.  For any question related to the case consumers should call 1-800-354-8460.

The recall include the following product:

Product Description – Ultilet Insulin Syringe 30g ½ cc
Lot – 5GEXI
NDC # - 08326-3002-50

A single complaint and a reported event prompted a Company investigation, which is on going.  The compliant stated that when the syringe was used, the color of the insulin solution entering the syringe chamber changed.  The firm decision to recall the product lot is voluntary.  The firm has placed all inventory of the product on hold.  FDA has been apprised of this action.

No serious injury has been reported.  No other lot is included on this Recall.

Boca Medical method of distribution is through wholesalers.  This product is sold by prescription orders.  This product has been distributed to the following states: FL, NY, MA, AL, SC, NC, CO, TX, MI, AR.

Boca Medical is notifying its wholesalers by fax and is arranging for the return of the recalled product from retail and consumer level.

 

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Did You Know?    
 
 
Many over the counter drugs were once prescription drugs
Americans buy about 5 billion over-the-counter drugs each year, according to government estimates, to treat their headaches, heartburn, coughs and colds, and other routine health problems. According to the Consumer Healthcare Products Association, a trade

 


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Drug Litigation Terms

 


Today's Terms

Marketing Status

Definition:
Marketing status indicates how a drug product is sold in the United States.

Discontinued Drug

Definition:
A discontinued drug is a drug product that has been removed from the market in the United States for reasons other than safety or effectiveness.

Label

Definition:
The FDA approved label is the official description of a drug product which includes indication (what the drug is used for); who should take it; adverse events (side effects); instructions for uses in pregnancy, children, and other populations; and safety

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Topics Related to Drug Litigation:

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