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Voluntary Recall of Three Detect Covid-19 Test Lots

Murilo Freitas - 19:31, 11 de diciembre de 20221,199
Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, our molecular, over-the-counter test used to identify SARS-CoV-2 (the virus that causes Covid-19) in self-collected nasal swabs. The recall affects a total of 11,102 tests shipped to customers from July 26th, 2022 thro

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-three-detect-covid-19-test-lots

 
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Remel, Inc Recalls Thermo Scientific Gram Negative IVD AST Sensititre Plate for risk of potential false susceptible results

Murilo Freitas - 05:00, 8 de diciembre de 20221,392
Thermo Scientific Gram Negative IVD AST Sensititre Plate is being recalled for a risk of potential false susceptible results when tested with certain antibiotics.

http://www.fda.gov/medical-devices/medical-device-recalls/remel-inc-recalls-thermo-scientific-gram-negative-ivd-ast-sensititre-plate-risk-potential-false

 
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Dewei Medical Equipment Co. Recalls DNA/RNA Preservation Kits That Are Not Authorized, Cleared, or Approved by the FDA

Murilo Freitas - 05:00, 7 de diciembre de 20221,461
Dewei Medical Equipment is recalling DNA/RNA Preservation Kits because they were distributed to U.S. customers without FDA authorization, clearance, or approval.

http://www.fda.gov/medical-devices/medical-device-recalls/dewei-medical-equipment-co-recalls-dnarna-preservation-kits-are-not-authorized-cleared-or-approved

 
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