CLASS III Food recall · Reported 2 Dec 2015 · FDA Enforcement Report
Curley Parsley recalled by MR Cuta
MR Cuta is recalling Curley Parsley, distributed in Texas. The recall was initiated on 18 Sep 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-0266-2016
- FDA event ID
- 72222
- Recalling firm
- MR Cuta, Dallas, TX
- Brand
- Curley Parsley
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 18 Sep 2015
- FDA classified
- 21 Nov 2015
- Reported
- 2 Dec 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Packaging Defects
- Product category
- Fish
Timeline
| 18 Sep 2015 | Recall initiated by company | |
| 21 Nov 2015 | Classified by FDA | +64 days |
| 2 Dec 2015 | Published in enforcement report | +11 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 the pesticides propanocarb and trifloxystrobin.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Curley Parsley 4/5 lb packaged in cardboard box, UPC code 740695801109
Where it was distributed
Dallas, TX
Questions about this recall
Is Curley Parsley recalled?
Yes. MR Cuta recalled Curley Parsley on 18 Sep 2015. The recall is Class III and its status is Terminated. Recall number F-0266-2016.
Why was it recalled?
Product tested positive for the pesticides propanocarb and trifloxystrobin.
Which lots are affected?
-0915, 09-15, 0915-
Where was it sold?
Dallas, TX
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 21 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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