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Microbiologics Recalls
66 recalls on record · July 11, 2012 to December 31, 2025 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 26, 2019Medical DevicesFDA
Microbiologics Inc recalls Cepheid Xpert C. difficile/Epi Control Panel
Hazard: Product is labeled with expiration date of 2021-10-31, should be 2021-03-31.
June 12, 2019Medical DevicesFDA
Microbiologics Inc recalls Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: 70845357041233 Product Usage: On April 9, 2019, M
Hazard: Product with incorrect shelf life.
June 12, 2019Medical DevicesFDA
Microbiologics Inc recalls Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019, Micro
Hazard: Product with incorrect shelf life.
March 13, 2019Medical DevicesFDA
Microbiologics Inc recalls Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
Hazard: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced expiration date from 24 months to 13 months.
April 3, 2013Medical DevicesFDA
Microbiologics Inc recalls Microbiologics KWIK-QC SLIDES ( KWIK-QC Acid Fast Stain Slides and KWIK-QC Mycobacterium Slides). Slide preparations
Hazard: Microbiologics Inc is initiating a voluntary recall on products KWIK-QC Acid Fast Stain Slide, SL42-10 and KWIK-QC Mycobacterium, SL43-10. These products are being recalled because the control organisms are not properly fixated on the slide, which may cause the user to unintentionally contaminate the patient area of the slide by flooding the control well with stain. This contamination could pote
July 11, 2012Medical DevicesFDA
Microbiologics Inc recalls Microbiologics 217 Osseo Avenue North, St. Cloud, MN 56303, Gram Stain Control Slides, SLO3-10, ATCC Licensed Derivativ
Hazard: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides. This product gram negative control organism (E.coli) is not properly fixated on the slide, which may cause the user to unintentionally contaminate the patient area of the slide by flooding the control well with stain. This contamination could potentially lead to misdiagnosis and improper treatment of a patient.