Check the Batch

RECALLING FIRM / COMPANY

Green Mountain Coffee Roasters Recalls

Are there any recent FDA recalls involving Green Mountain Coffee Roasters?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

4 FDA product recordsLatest initiation: Jan 10, 2014

Same product name.
Different batch.
Check the label.

All FDA recall records involving Green Mountain Coffee Roasters

Initiated in 2013. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

3 recall recordsPage 1 of 1
Class III
FDA status: Terminated

Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes)

Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

OtherView details →
Class III
FDA status: Terminated

Tully's House Blend Decaffeinated K-Cup¿ Packs (12-ct retail box) Product Code: 8803

Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

OtherView details →
Class II
FDA status: Terminated

Master Cases, Product Code #8534 (6-12 count retail boxes) Label of master case bears the name: Donut House K -Cup…

Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee.

OtherView details →

Found your product? Now check the codes.

Same product name. Different batch. Details matter.

→