Remel recalls Sensititre STP6F Gram Negative IVD AST plates with specific lot numbers due to risk of false susceptible results for certain bacteria when tested with specific antibiotics.
An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
Remel is recalling Sensititre STP6: Gram Negative IVD AST plates that may give false results for certain bacteria when tested with specific antibiotics. This could lead to incorrect treatment decisions if used in medical testing.
The plates may produce false susceptible results for specific bacteria when tested with certain antibiotics. This means the test might incorrectly show bacteria as sensitive to antibiotics when they are not, potentially leading to inappropriate treatment choices.
Healthcare professionals using these plates for bacterial testing are most at risk. Patients relying on accurate test results could be affected if the false results lead to incorrect treatment.
Check the lot numbers on the plate: B2314, B2174, B2036, B1346, B1183, B1115, or B1027. These plates are sold by Remel for medical testing.
Identify the lot number on the Sensititre STP6F plate to see if it matches the recalled numbers: B2314, B2174, B2036, B1346, B1183, B1115, or B1027.
The recall affects Proteus spp., Providencia spp., Morganella Morganii, and other bacteria in the Proteae Tribe.
The plates may give false results when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam, and aztreonam.
The recall does not require immediate stop use; check the lot numbers to determine if your plate is affected.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-0334-2023 — Remel Remel Hello, I own a Remel that is covered by recall Z-0334-2023 from Remel. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
