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Microtek Medical, Inc.

Microtek Medical, Inc. Recalls

All product recalls associated with Microtek Medical, Inc..

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Recall Summary

Total Recalls

1000

Past Year

742

Class I (Serious)

175

Most Recent

Jan 2026

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 521–540 of 11123 recalls

Microtek Patient Drape (Microtek) – Sterility Concern (2025)

Due to non-sterile products being labeled as sterile

Moderate

FDAApr 13, 2025AL, AR, CA +17 more• Microtek Medical, Inc.

Volkswagen ID. Buzz (Volkswagen) – Brake Warning Light (2025)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2025 ID. Buzz vehicles. The brake system warning light on the instrument panel display may be the incorrect symbol and color. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 135, "Light Vehicle Brake Systems" and 101, "Control and Displays."

Moderate

NHTSAApr 10, 2025Nationwide• VOLKSWAGEN

Tequila Lime Base (Bakkavor Foods) – wood pieces (2025)

Foreign Object - Wood. The firm was notified by their supplier that the product may contain pieces of wood.

Class IIModerate

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Page 27 of 557Next

FDA

Apr 10, 2025

AL, CA, FL +1 more

• Bakkavor Foods USA, Inc.

PiezoWave 2 Control Unit (Richard Wolf) – Capacitor Failure (2025)

Fire/Burn Risk

The high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell. In extremely rare instances a capacitor may cause a spark or excessive heat when an internal capacitor failure occurs.

High

FDAApr 9, 2025GA• Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany

Artix MT Thrombectomy Device (Inari) – Vessel Range (2025)

Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.

Low

FDAApr 8, 2025Nationwide• Inari Medical Oak Canyon

REMISOL Advance Software (Beckman Coulter) – Date Processing (2025)

Laceration Risk

Due to a software issue, the software may incorrectly process the date of birth (DoB) received from the Laboratory Information System (LIS) and when the DoB is set to 01/01/1900 or left empty, REMISOL Advance may incorrectly identify a patient as a newborn, affecting the execution of validation rules based on incorrect reference ranges. The test results are not changed by this software defect and are accurately displayed by REMISOL Advance; however, the evaluation flagging of the results may be affected. This issue may lead to wrong reference range calculations and can result in erroneous flagged results being auto validated and uploaded to LIS.

Moderate

FDAApr 8, 2025Nationwide• Beckman Coulter Inc.