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Updated: 2007-03-20

Model Device Recall Press Release

FOR IMMEDIATE RELEASE                                                      DATE

Device Firm Issues Nationwide Recall of Product

(WORD Version)

Company Name, City, State, is initiating a nationwide recall of quantity and type of product. The products have been found to describe problem, which has/potentially could result in describe public healthrisk.

Consumers who have product which is being recalled should stopusing/return/replace/throw away/contact their doctor, etc.

The recall includes the following styles/models/codes/ID numbers, etc.:

Name of product Model #

Name of product Model #

Name of product Model #

The firm voluntarily recalled the products after learning (fill in). FDA has been apprised of this action.

Brief explanation about what is known about the problem. Number, type and status of any injuries that have been CONFIRMED to date (e.g., “No injuries have been reported to date.”)

Product was distributed to describe type of outlets, states and areas, and method of distribution. It can be identified by provide additional details about how product can be identified by users.

Company is notifying its distributors and customers by describe method and is arranging for return/replacement/retrofit, etc. of all recalled products.

Consumers with questions may contact the company at 1-800-xxx-xxx.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.