Drugs & medicalClass II

Cepheid recalls Cepheid, Sample Collection Device, Part: 900-0370

Specimen collection device may leak after the patient sample swabs have been inserted into the test tubes, which could result in biohazard exposure, cross contamination causing false positive results for other…

Read the official notice →
Date
2024-08-21
Country
United States
Brand
Cepheid
Product
Cepheid, Sample Collection Device, Part: 900-0370
Classification
Class II
Units
Worldwide distribution: US (nationwide): IL, TX, OH, LA, NY, CA, MD, IA, MN,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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