Thermo Fisher recalls 50 units of Remel SUPERPACK CS/500 SEG/FL: May fail performance testing for Staphylococcus aureus resistance. Consumers should check product labels for REF R01626 and lot 307200.
Product may fail performance testing for S aureus ATCC 43300.
Thermo Fisher is recalling 50 units of Remel SUPERPACK CS/5:00 SEG/FLASK (REF R01626) because they may fail performance testing for Staphylococcus aureus. This could lead to inaccurate results in testing for antibiotic resistance.
The product may not properly detect Staphylococcus aureus resistance to penicillinase-resistant penicillins. This could result in inaccurate test results for antibiotic resistance, but does not cause physical harm.
Users of this lab culture product for Staphylococcus aureus testing may be affected. Laboratory staff and researchers using the product for antibiotic resistance screening are most at risk.
Check for the product label 'REMEL MH W/OXACILLIN' and the reference number REF R01626. The lot number is 307200. This product is sold for qualitative testing of Staphylococcus aureus.
Look for the label 'REMEL MH W/OXACILLIN' and reference number REF R01626 with lot 307200.
Thermo Fisher is recalling 50 units of Remel SUPERPACK CS/500 SEG/FLASK (REF R01626) with lot number 307200.
The product may fail performance testing for Staphylococcus aureus, which could lead to inaccurate results in antibiotic resistance screening.
Check the product label for 'REMEL MH W/OXACILLIN' and reference number REF R01626 with lot 307200. No specific action is required beyond checking the label.
We’ve drafted a message you can send Thermo Fisher to request your refund or repair — edit it as you like.
Subject: Recall Z-2137-2018 — Thermo Fisher Thermo Fisher Hello, I own a Thermo Fisher that is covered by recall Z-2137-2018 from Thermo Fisher. 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.
