FDA recall record

Paragon Foods Warrendale, PA 15086 Label: Paragon recall — FDA F-0362-2018

Paragon Wholesale Foods Corp., of Warrendale, PA, is recalling several lots of 1.7 ounce Broccoli Florets in response to a nationwide recall by one of its…

Class Iclassification
F-0362-2018official record ID
Nov 29, 2017report date

Recall record at a glance

Official recordF-0362-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmParagon Foods
Report dateNov 29, 2017
Recall initiation dateOct 19, 2017
Quantity37 cases (50/1.7 oz.); 4 X 5 lb. bags
LocationWarrendale, PA, United States

Official product description

Paragon Wholesale Foods, Warrendale, PA 15086 Label: Paragon; Best if used by 10/16/17; Broccoli Florets 1/2 Cup 50/1.7 oz.; X0011932 17279; UPC: 86870 03200 AND Paragon; Best if used by: 10/23/17; Broccoli Florets 1/2 Cup 50/1.7 oz.; X0012592 17286; UPC: 86870 03200 Bulk: Paragon Wholesale Foods, Warrendale, PA 15086 Paragon Broccoli 1/4" Diced FFM. 5 lbs; X0012561 17285; UPC: 86870 08284; Best if used by: 10/24/17

Why the product was recalled

Paragon Wholesale Foods Corp., of Warrendale, PA, is recalling several lots of 1.7 ounce Broccoli Florets in response to a nationwide recall by one of its suppliers, Mann Packing (Salinas, CA) because they have the potential to be contaminated with Listeria monocytogenes

Distribution information

Pittsburgh and Butler County in PA

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.