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Microbiologics Inc

Microbiologics Inc Recalls

All product recalls associated with Microbiologics Inc.

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Recall Summary

Total Recalls

1000

Past Year

442

Class I (Serious)

138

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1021–1040 of 7663 recalls

KWIK-STIK QC Set (Microbiologics) – Missing Strain (2023)

One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains, 6018P Parabacteroides distasonis.

Low

FDAAug 14, 2023Nationwide• Microbiologics Inc

Mercedes-Benz E 350 (Mercedes-Benz) – Blindspot Sensor Error (2023)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2023 E450, E350, AMG E63 S, AMG E53, CLS450, AMG GT53, and AMG GT43 vehicles. Due to a software error, the exit warning system audio and visual warnings may fail to alert occupants about approaching vehicles.

Moderate

NHTSAAug 11, 2023Nationwide• MERCEDES-BENZ

Functional MR Software (Olea Medical) – Export Error (2023)

When exporting regions of interest in DICOM SEGMENTATION format, when simultaneously exporting multiple volumes of interest, a functional magnetic resonance software bug may cause file contents and associated series descriptions to not match, which could lead to a misinterpretation of clinical data.

1...50 515253 54...384

Page 52 of 384Next

Moderate

FDAAug 10, 2023MA, MI• OLEA MEDICAL 93 AVANUE DU SORBIER, ZONE ATHELIA IV LA CIOTAT France

Knorr Estrellitas Tomato Soup Mix (Unilever) – undeclared egg (2023)

Undeclared Egg

Undeclared egg

Class IIModerate

FDAAug 10, 2023Nationwide• Conopco DBA Unilever

Knorr Letras Tomato Soup Mix (Unilever) – undeclared egg (2023)

Undeclared Egg

Undeclared egg

Class IIModerate

FDAAug 10, 2023Nationwide• Conopco DBA Unilever

Knorr Fideos Tomato Soup Mix (Unilever) – undeclared egg (2023)

Undeclared Egg

Undeclared egg

Class IIModerate

FDAAug 10, 2023Nationwide• Conopco DBA Unilever

Oculus Pentacam AXL Wave (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

Moderate

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Oculus Myopia Master (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

Moderate

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Oculus Pentacam AXL (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

Moderate

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

EQE 350 4MATIC (MERCEDES-BENZ) – roof frame weakness (2023)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2023 AMG EQE, EQE 500, and EQE 350 vehicles. The absorbers in the roof frame may not be secured properly and can detach during window air bag deployment.

Moderate

NHTSAAug 4, 2023Nationwide• MERCEDES-BENZ

S 580 (MERCEDES-MAYBACH) – trunk wiring issue (2023)

Fire/Burn Risk

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2022-2023 Maybach S580 and Maybach S680 vehicles. The 12-Volt ground connection in the trunk may not be secured properly, which can impair the electronic stability program (ESP) or result in the ground connection overheating.

High

NHTSAAug 4, 2023Nationwide• MERCEDES-MAYBACH

Avent Baby Monitors (Philips) – Burn risk (2023)

Fire/Burn Risk

This recall involves Philips Avent video baby monitors used to remotely monitor infants. They consist of a Baby Unit (camera) and a Parent Unit (monitor) pair. The monitor has a 3.5-inch color screen. The recalled baby monitors include models SCD630 and SCD843 only, manufactured between March 2016 and December 2019. The model numbers and production date codes, in day-month-year format, are located on the bottom of the Parent Unit. The monitors and camera are white. Philips Avent is printed on the front.

High

CPSCAug 3, 2023Nationwide• Philips Consumer Lifestyle B.V., of The Netherlands

3T Heater Cooler System (LivaNova) – maintenance schedule error (2023)

The firm's labeling (Quick Reference Guide) contains incorrect information in the maintenance schedule for the Heater-Cooler device.

Low

FDAAug 3, 2023Nationwide• LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany

Blueberry Bagels (Crispy Bagel) – Undeclared sesame (2023)

Undeclared Allergen

Undeclared sesame

Class IIModerate

FDAAug 2, 2023IN, MD, NC +1 more• Crispy Bagel Co., Inc.

Sprinter (CREATIVE MOBILE) – recreational vehicle problem (2023)

Fire/Burn Risk

Airstream, Inc. (Airstream) is recalling certain 2019-2023 Ford Transit, 2020 RAM, and 2020-2022 Sprinter recreational vehicles upfitted by Creative Mobile Interiors. The fuel hose between the inline fuel filter and the injection pump module (IMP) may have inadequate clamp force, possibly resulting in a gasoline leak.

High

NHTSAJul 27, 2023Nationwide• CREATIVE MOBILE INTERIORS

Zenition 70 (Philips) – Radiation Exposure Risk (2023)

Philips has become aware of the potential for unintended radiation exposure with Zenition 70 systems with Vascular Extension option and a Wireless Foot Switch.

Moderate

FDAJul 20, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Azurion (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Allura Xper Series (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

MultiDiagnost-Eleva (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Fosfomycin Tromethamine Granules (Ascend) – Impurity Specification Failure (2023)

Failed Impurities/Degradation Specifications: Out-of-specification results observed for the organic impurities test at 6 months, RT Stability.

Class IIILow

FDAJul 18, 2023Nationwide• Ascend Laboratories, LLC