CLASS III Food recall · Reported 19 Jun 2024 · FDA Enforcement Report

TriyBrewed Coffee Concentrate, amber to case recalled by Waco Bottling

Waco Bottling is recalling TriyBrewed Coffee Concentrate, amber to case. The recall was initiated on 10 May 2024 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesOWB29823 EXP 10/24/24
Quantity recalled321 cases / 3852 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1359-2024
FDA event ID
94689
Recalling firm
Waco Bottling, Woodway, TX
Classification
Class III
Status
Terminated
Recall initiated
10 May 2024
FDA classified
13 Jun 2024
Reported
19 Jun 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Coffee

Timeline

10 May 2024Recall initiated by company
13 Jun 2024Classified by FDA+34 days
19 Jun 2024Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

No ingredient statement and no nutrition label

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

TriyBrewed Coffee Concentrate 6oz/177ml, amber glass bottle, 6pcs to case

Where it was distributed

Throughout the USA via Amazon

Stores named: Amazon, Online Retailers

Questions about this recall

Why was it recalled?

No ingredient statement and no nutrition label

Which lots are affected?

OWB29823 EXP 10/24/24

Where was it sold?

Throughout the USA via Amazon

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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