A soap recall that a company initiated back in August has expanded to more than 30 personal care products. DermaRite industries has expanded a recall on soap products to include more than 30 personal care products, from shampoos to lotions.
More items including sanitizer, shampoo, lotions and deodorant have been impacted over concerns that using them could result in "serious and life-threatening infections" like sepsis, according to NBC Chicago.
The recall, originally issued in July, included four products from DermaRite Industries, LLC but now number of recalled products has now expanded to more than 30 products.
The company voluntarily pulled back a batch of its soaps after warning that contamination with Burkholderia cepacia complex bacteria could trigger infections in open wounds and, in severe cases, lead to potentially life-threatening sepsis.
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Burkholderia cepacia complex, also called B. cepacia or Bcc, is a group of bacteria that can cause infections in healthcare settings. B. cepacia germs can be resistant to antibiotics, making them difficult to treat, the CDC says.
Symptoms of infection can vary, "ranging from no symptoms to serious respiratory infections, especially in patients with cystic fibrosis or other chronic lung disease," according to the CDC. Other symptoms may include things like fever or fatigue, the agency notes.
In the United States, people in healthcare settings and those with weakened immune systems or chronic lung diseases, particularly cystic fibrosis, are at highest risk of infection with B. cepacia complex. B. cepacia complex poses little medical risk to healthy people, the health agency says.
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Contact with contaminated surfaces
Contact with contaminated equipment
Person-to-person transmission, more commonly in patients with cystic fibrosis.
Risks for patients and caregivers can be reduced by following these steps:
Wash hands thoroughly, especially before and after caring for wounds or handling medical devices.
Remind visitors or others to clean their hands before touching the patient or any medical equipment.
Keep wounds and devices that are inside or connected to the body away from non-sterile water.
Allow healthcare staff to clean the patient’s room daily while in a medical facility.
For healthcare providers, one must always follow infection control guidelines to prevent the spread of germs and protect patients.
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Anyone who experiences health issues after using the product should contact their physician or healthcare provider, the recall stated. Those with questions regarding the recall can call (973) 569-9000 x104 between 8 a.m. and 4 p.m. CT Monday through Friday or email voluntary.action@dermarite.com.
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.
More items including sanitizer, shampoo, lotions and deodorant have been impacted over concerns that using them could result in "serious and life-threatening infections" like sepsis, according to NBC Chicago.
The recall, originally issued in July, included four products from DermaRite Industries, LLC but now number of recalled products has now expanded to more than 30 products.
The company voluntarily pulled back a batch of its soaps after warning that contamination with Burkholderia cepacia complex bacteria could trigger infections in open wounds and, in severe cases, lead to potentially life-threatening sepsis.
ALSO READ: After Charlie Kirk shooting, Tyler Robinson’s alt-right links to Nick Fuentes spark outrage, activist breaks silence
What is Burkholderia cepacia complex?
According to the Centers for Disease Control and Prevention, Burkholderia cepacia complex, also called B. cepacia or Bcc, is "a group of bacteria commonly found in soil and water," and such germs can be resistant to antibiotics.Burkholderia cepacia complex, also called B. cepacia or Bcc, is a group of bacteria that can cause infections in healthcare settings. B. cepacia germs can be resistant to antibiotics, making them difficult to treat, the CDC says.
Symptoms of infection can vary, "ranging from no symptoms to serious respiratory infections, especially in patients with cystic fibrosis or other chronic lung disease," according to the CDC. Other symptoms may include things like fever or fatigue, the agency notes.
In the United States, people in healthcare settings and those with weakened immune systems or chronic lung diseases, particularly cystic fibrosis, are at highest risk of infection with B. cepacia complex. B. cepacia complex poses little medical risk to healthy people, the health agency says.
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How does Burkholderia cepacia complex spread?
Exposure from water, soil or aqueous (watery) environmentsContact with contaminated surfaces
Contact with contaminated equipment
Person-to-person transmission, more commonly in patients with cystic fibrosis.
Risks for patients and caregivers can be reduced by following these steps:
Wash hands thoroughly, especially before and after caring for wounds or handling medical devices.
Remind visitors or others to clean their hands before touching the patient or any medical equipment.
Keep wounds and devices that are inside or connected to the body away from non-sterile water.
Allow healthcare staff to clean the patient’s room daily while in a medical facility.
For healthcare providers, one must always follow infection control guidelines to prevent the spread of germs and protect patients.
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What to do if you have any of the recalled items?
The company said no reports of infections have been reported so far in connection with the recalled products. But it has requested customers and distributors to "immediately examine available inventory and destroy all affected products in accordance with each facility's process."Anyone who experiences health issues after using the product should contact their physician or healthcare provider, the recall stated. Those with questions regarding the recall can call (973) 569-9000 x104 between 8 a.m. and 4 p.m. CT Monday through Friday or email voluntary.action@dermarite.com.
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.