U. S. GOV T AWARDS RETRACTABLE TECHNOLOGIES SECOND SAFETY SYRINGE CONTRACT UNDER BUSH GLOBAL HIV/AIDS

U. S. GOV T AWARDS RETRACTABLE TECHNOLOGIES SECOND SAFETY SYRINGE CONTRACT UNDER BUSH GLOBAL HIV/AIDS INITIATIVE

LITTLE ELM, TEXAS, Nov. 2, 2005-Retractable Technologies, Inc. (AMEX: RVP) announced today

that it has been awarded its second major U.S. government contract to provide VanishPoint safety syringes under the Bush Administration s Global HIV/AIDS initiative (President s Emergency Plan for AIDS Relief). Under the contract,

awarded in connection with Phase II of the syringe program, Retractable will supply at least 11.7 million of its patented automated retraction syringes to Haiti and seven African nations: Botswana, Cote d Ivoire, Ethiopia, Kenya, Nigeria,

Tanzania, and Uganda.

Retractable received its first contract through the

program in August 2004; the new award includes Uganda and Haiti in addition to the original six African countries. Retractable is the only U.S. maker of non-reusable safety syringes to receive a contract under the President s Emergency Plan.

Worldwide, it is also the largest supplier of such syringes for the initiative, which was launched by President Bush in 2003 as a rapid intervention strategy to prevent seven million new HIV infections in 14 AIDS-ravaged countries in Africa and the

Caribbean. Since 1999, Retractable has also been marketing its safety needle devices to private hospitals and government healthcare facilities in South Africa through a local distributor.

Thomas J. Shaw, president and CEO of Retractable, said that This new award demonstrates that VanishPoint syringes are the safety

syringe of choice under the President s Global HIV/AIDS initiative. The fact that all of the countries that ordered VanishPoint syringes in significant volumes in Phase I of the program have requested them again in Phase II speaks louder

than words about the value of our technology in protecting African patients and healthcare workers from potentially deadly contaminated needles. He added: Once again, I d like to thank the Bush Administration and Congress for

launching this landmark humanitarian program.

Countries included in the

initiative were given the opportunity to evaluate and select the syringes they preferred from among all of those that met the program s bid requirements. International health organizations have long recognized that the reuse of syringes in

these countries plays a significant part in the HIV pandemic. VanishPoint safety devices not only prevent reuse but also virtually eliminate accidental needlestick injuries and minimize hazardous medical waste, a major problem in developing

In a related development, Retractable also announced that the World

Health Organization (W.H.O.) has designated its VanishPoint devices as pre-qualified under the international agency s PQS (Performance Quality System) program. This important credential paves the way for the possible future

selection of VanishPoint syringes for programs sponsored by UNICEF and other United Nations and international agencies.

Retractable Technologies, Inc. manufactures and markets VanishPoint automated retraction safety syringes and blood collection devices, which virtually eliminate

health care worker exposure to accidental needlestick injuries. These revolutionary devices use a patented friction ring mechanism that causes the contaminated needle to retract automatically from the patient into the barrel of the device, a feature

that is designed to prevent reuse. VanishPoint safety needle devices are distributed by various specialty and general line distributors. For more information on Retractable, visit our Web site at www.vanishpoint.com. Forward-looking statements

in this press release are made pursuant to the safe harbor provision of the Private Securities Litigation Reform Act of 1995 and reflect the Company s current views with respect to future events. The Company believes that the expectations

reflected in such forward-looking statements are accurate. However, the Company cannot assure you that such expectations will materialize. The

Company s actual future performance could differ materially from such statements. Factors that could cause or

contribute to such differences include, but are not limited to: the impact of dramatic increases in demand; the Company s ability to quickly increase its production capacity in the event of a dramatic increase in demand; the Company s

ability to access the market; the Company s ability to decrease production costs; the Company s ability to continue to finance research and development as well as operations and expansion of production; the increased interest of other

larger market players, specifically BD, in providing safety needle devices to their customers; and other risks and uncertainties that are detailed from time to time in the Company s periodic reports filed with the Securities and Exchange

Vice President and Chief Financial Officer

(888) 806-2626 or (972) 294-1010

Communications Director

(212) 490-0811 or (214) 912-7415 (cell)