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You are here: Home / Food Recalls / FDA Press Releases / U.S. Deer Antler EX. & IM., INC. Announces The Recall Of Herbal Tea Varieties In Pouches Due To Risk For Clostridium Botulinum

U.S. Deer Antler EX. & IM., INC. Announces The Recall Of Herbal Tea Varieties In Pouches Due To Risk For Clostridium Botulinum

May 4, 2017 By The FDA Leave a Comment

U.S. Deer Antler Ex. & Imp., of Los Angeles, CA is recalling a variety of Herbal Teas prepared on premises between 4/1/17 and 4/30/17 in cooperation with an inspection made by the California Department of Public Health. The aforementioned Herbal Teas, especially those with low-acidity held at room temperature, were not produced according to approved guideline, making them susceptible to contamination by Clostridium botulinum. 

Below are the product descriptions and photographs:

Products Packaging Cases
Herbal Tea Variety Batches prepared on premise between 4/1/17 – 4/30/17 120 ml/ Pouch 40 Pouches / Case

The Herbal Teas were distributed to individual customers and acupuncturists in California, Florida, Illinois, Maryland, North Carolina, Texas, and Virginia.

Symptoms of Clostridium botulinum typically begin with blurred or double vision followed by trouble speaking, swallowing; and progression to muscle weakness starting in the upper body, moving downward.  Botulism can lead to life-threatening paralysis of breathing muscles requiring support with a breathing machine (ventilator) and intensive care. https://www.cdph.ca.gov/HealthInfo/discond/Pages/Botulism.aspx

People experiencing these symptoms who have recently consumed these Herbal Teas should seek immediate medical attention.

In its ongoing cooperation with the California Department of Public Health, U.S. Deer Antler Ex. & Imp., Inc. has immediately segregated its entire inventory of Herbal Tea varieties, and is notifying consumers and customers not to consume potentially-contaminated product. Furthermore, U.S. Deer Antler Ex. & Imp. Inc. is voluntarily recalling all varieties of general Herbal Teas prepared on-site in the period of 4/1/17 to 4/30/17 to ensure consumer safety.

Consumers in possession of these products are to stop consumption and return unconsumed product to their original place of purchase.  

U.S. Deer Antler Ex. & Imp., Inc. will be sending recall notices to all of its direct customers.  Please contact Joong W. Park (323) 735-9665 for further information.

언론보도

미주녹용건재상사

보툴리눔균 감염우려가 있는 한약탕제 파우치 리콜안내

 

연락처: 중 박

전화번호:  (323) 735-9665

긴급고지 – 가주 로스엔젤레스

2017년 5월 1일

 

가주 로스엔젤레스에 위치하고 있는 미주녹용이 2017년 4월 1일부터 4월 30일 사이에 만들어진 여러 종류의 탕제 리콜을 시행하고 있다.

가주보건국의 감사에 따라 상기 기간에 만들어진 탕제들이 저산도와 상온에 보관 되어 허락된 지침에 따르지 않아 보툴리눔균에 오염될 가능성이 있다.

 

제품 설명 및 사진

 

 

제    품

포 장 단 위

수     량

탕제 (Herbal Tea Variety Batches)

 

120 ml /파우치

 

 

40 파우치 / 박스

 

 

이 탕제들은 남가주 및 플로리다, 일리노이즈, 메릴랜드, 노스캐롤라이나, 텍사스, 버지니아주에 있는 한의원들과 고객에게 판매되었다.

 

보툴리눔균의 감염 증상은 처음에 시야가 흐려지거나 혹은 이중으로 보이는 증상이 시작되고 이어서 말하기와 음식을 삼키는데 어려움이 따르며, 상체에서 하체로 내려가는 근육약화 증상으로 진행된다. 보툴리즘은 치명적인 호흡근육의 마비로 인해 인공호흡기 사용 같은 적극적 치료를 해야 할 수도 있다.

 

최근에 이 탕제를 복용하고 상기와 같은 증상을 경험한 사람은 즉각적인 치료를 받아야 한다.

 

가주 보건국의 요청에 따라 미주녹용은 만들어진 모든 탕제를 폐기 조치하고 감염될 가능성이 있는 제품이 사용되지 않도록 소비자들에게 알리고 있다. 나아가서 미주녹용은 2017년 4월 1일부터 4월 30일 사이에 제조된 탕제에 대하여 자발적 리콜을 실시하고 있다.

 

이 제품을 구입한 소비자들은 복용을 중지하고 구입한 곳에 나머지를 반품하면

된다.

 

미주녹용은 거래하는 모든 소비자들에게 리콜고지서를 발송하고 있다. 보다 자세한 정보는 중 박 (323) 735-9665 에게 문의하기를 바란다.

###

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Filed Under: FDA Press Releases

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