CLASS III Food recall · Reported 25 May 2016 · FDA Enforcement Report
Manischewitz Pistachio Orange Macaroons recalled by R.A.B. Food Group
R.A.B. Food Group is recalling Manischewitz Pistachio Orange Macaroons, distributed in California, Florida, Illinois, Maryland, New York, Pennsylvania. The recall was initiated on 30 Mar 2016 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-1333-2016
- FDA event ID
- 73711
- Recalling firm
- R.A.B. Food Group, Newark, NJ
- Brand
- Manischewitz
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 30 Mar 2016
- FDA classified
- 13 May 2016
- Reported
- 25 May 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Herbal Supplements
Timeline
| 30 Mar 2016 | Recall initiated by company | |
| 13 May 2016 | Classified by FDA | +44 days |
| 25 May 2016 | 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
Manischewitz Pistachio Orange macaroons may contain pistachio shell fragments.
Product as listed by the FDA
Manischewitz Pistachio Orange Macaroons 10 oz. Distributed by: The Manischewitz Company Newark, NJ 07105 Product of USA UPC 0-7270000119-6
Where it was distributed
CA, FL, IL, MD, NY, PA and foreign
Questions about this recall
Why was it recalled?
Manischewitz Pistachio Orange macaroons may contain pistachio shell fragments.
Which lots are affected?
Lot #N5336A September 1, 2016
Where was it sold?
CA, FL, IL, MD, NY, PA and foreign
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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