Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Tosoh Bioscience Inc

Tosoh Bioscience Inc Recalls

All product recalls associated with Tosoh Bioscience Inc.

Get alerts for this brand

Recall Summary

Total Recalls

710

Past Year

Class I (Serious)

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 301–320 of 710 recalls

Tosoh Bioscience Inc: Tosoh Bioscience AIA-PACK BHCG Calibration Verification T...

Decreased stability for five (5) lots of Calibrator Sets and Calibration Verification Test Sets, resulting in a decrease measured concentration of HCG up to 20%.

FDAAug 7, 2020Nationwide• Tosoh Bioscience Inc

Integra LifeSciences Corp.: Integra Padgett Electric Dermatome Set - Product Usage: a...

lntegra LifeSciences has identified through a number of complaints that the handpiece cable melts following sterilization.

FDAAug 4, 2020Nationwide• Integra LifeSciences Corp.

Integra LifeSciences Corp.: 13 ft Handpiece Cable, component of the Dermatome Sets Mo...

lntegra LifeSciences has identified through a number of complaints that the handpiece cable melts following sterilization.

FDA

1...14 151617 18...36

Page 16 of 36Next

Aug 4, 2020

Nationwide

• Integra LifeSciences Corp.

Integra LifeSciences Corp.: Integra Padgett Dermatome Set - Product Usage: are intend...

lntegra LifeSciences has identified through a number of complaints that the handpiece cable melts following sterilization.

FDAAug 4, 2020Nationwide• Integra LifeSciences Corp.

Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom: Cytocell LPH533-A NUP98 Distal Probe Green - Product Usag...

A low risk of a false positive result being issued with a laboratory developed test (LDT) that utilizes the LPH533-A NUP98 Distal Probe Green.

FDAJul 17, 2020Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Qiagen Sciences LLC: QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IV...

There is an increased rate of potential false positive results for the Influenza A (no subtype) target, which may lead to 1) inappropriate antiviral use, 2) erroneous or delayed differential diagnosis and missing of an alternative diagnosis.

FDAJul 15, 2020Nationwide• Qiagen Sciences LLC

Tosoh Bioscience Inc: AIA-900 Analyzer, Part no. 022930, UDI 04560189283992

The Substrate Monitoring System in the AIA-900 Analyzer did not detect an empty substrate bottle. The issue may lead to erroneous immunoassay test results.

FDAMay 22, 2020Nationwide• Tosoh Bioscience Inc

Wintergreen Essential Oil (Aromatics International) - Packaging Concern (2020)

This recall involves Aromatics International Wintergreen Essential Oil in 5 mL, 15 mL, 30 mL, and 100 mL glass amber bottes with a black continuous thread cap. The bottles have a white label with the firm's green logo on the front. UPC codes are listed on the 5 mL (817697021443) and 15 mL (817697021375) along the bar code. The batch numbers WIN-104 and WIN-105 are listed on a dot sticker located on the cap.

CPSCMay 14, 2020Nationwide• Aromatics International LLC, of Florence, Mont.