COOK VANDERGRIFT INC.
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (2)
Devices registered here (1)
- Microtools, Assisted Reproduction (Pipettes)Product code MQH (opens in a new tab) · Class II · Obstetrics/Gynecology · 21 CFR 884.6130
Recalls & enforcement
- Class IIOngoing2023-07-24Sterility of device may be compromised due to breach of the chevron seal of the packaging
FDA inspections (2)
- NAI2018-09-12No Action Indicated · Compliance: Devices
- NAI2016-10-21No Action Indicated · Compliance: Devices
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “COOK VANDERGRIFT INC. (FEI 2522007) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2522007-cook-vandergrift-inc/
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