Turbare Manufacturing recalls

Turbare Manufacturing has 1 recall on record with the FDA and USDA, the earliest in 2025 and the latest reported on 5 Mar 2025. The most frequent reason is sterility.

Total recalls1since 2025
Last 12 months0reported
Class I00% of total
Ongoing0latest 5 Mar 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why turbare manufacturing is recalled

Product types

By year

All turbare manufacturing recalls, newest first

1 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIAvastin 1.25 mg/ in Syringe recalled by Turbare ManufacturingTurbare ManufacturingSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.