CLASS II Food recall · Reported 7 Jun 2023 · FDA Enforcement Report
Trader Joes Instant Cold Brew Coffee recalled by Regal Trading
Regal Trading is recalling Trader Joes Instant Cold Brew Coffee, distributed in 7 states. The recall was initiated on 26 Apr 2023 and the FDA has classified it as Class II.
Check your package
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-0956-2023
- FDA event ID
- 92326
- Recalling firm
- Regal Trading, Totowa, NJ
- Brand
- Trader Joes
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Apr 2023
- FDA classified
- 26 May 2023
- Reported
- 7 Jun 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Particulate Matter
- Product category
- Coffee
Timeline
| 26 Apr 2023 | Recall initiated by company | |
| 26 May 2023 | Classified by FDA | +30 days |
| 7 Jun 2023 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Presence of foreign material (glass particles) in product.
Product as listed by the FDA
Trader Joes Instant Cold Brew Coffee, 3.5 oz.(99g), 24 jars per case.
Where it was distributed
TX, CA, CT, PA, CA, FL, IL, WA
CaliforniaConnecticutFloridaIllinoisPennsylvaniaTexasWashington
Stores named: Trader Joe's
Questions about this recall
Why was it recalled?
Presence of foreign material (glass particles) in product.
Which lots are affected?
Mfg: 06/13/22, Exp: 6/13/24 Mfg: 11/26/22 Exp: 11/26/24 Mfg: 12/30/22 Exp: 12/30/24
Where was it sold?
TX, CA, CT, PA, CA, FL, IL, WA
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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