CLASS III Food recall · Reported 22 Jul 2015 · FDA Enforcement Report
International Whole Segments Mandarin Oranges In Light Syrup recalled
Sysco is recalling International Whole Segments Mandarin Oranges In Light Syrup, distributed in 8 states. The recall was initiated on 18 Jun 2015 and the FDA has classified it as Class III.
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-2844-2015
- FDA event ID
- 71538
- Recalling firm
- Sysco, Houston, TX
- Brand
- International
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 18 Jun 2015
- FDA classified
- 10 Jul 2015
- Reported
- 22 Jul 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Citrus
Timeline
| 18 Jun 2015 | Recall initiated by company | |
| 10 Jul 2015 | Classified by FDA | +22 days |
| 22 Jul 2015 | 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
Product tested positive for Carbendazim.
Product as listed by the FDA
Sysco International Whole Segments Mandarin Oranges In Light Syrup Net Wt. 6 LB 10 OZ (3.01 kg) NDC: 074865629065; 6 cans per case
Where it was distributed
GA, AL, FL, SC, TN, NC, MS, LA
AlabamaFloridaGeorgiaLouisianaMississippiNorth CarolinaSouth CarolinaTennessee
Questions about this recall
Why was it recalled?
Product tested positive for Carbendazim.
Which lots are affected?
Can Code: W29 02 20141119 601 Master Carton Code: 01765570 W29 02 20141119 601 GTIN UPC: 10074865629062
Where was it sold?
GA, AL, FL, SC, TN, NC, MS, LA
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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