FDA recall record

Power Selles Imports dba Culinary Collective Matiz Piparra Peppers are packaged in a clear recall — FDA F-0741-2023

A shard of glass being found in one of the jars.

Class IIclassification
F-0741-2023official record ID
Apr 26, 2023report date

Recall record at a glance

Official recordF-0741-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPower Selles Imports dba Culinary Collective
Report dateApr 26, 2023
Recall initiation dateMar 13, 2023
Quantity150 cases (5 jars per case, 4lb. per jar).
LocationLynnwood, WA, United States

Official product description

Matiz Piparra Peppers are packaged in a clear glass jar, net wt. 4lb. (1.8kg), drained wt. 25oz (700g). Product is shelf stable. UPC 832924005768. Produced By Conservas Rubio - Navarra, Spain. Imported By Matiz A Culinary Collective Company Lynnwood, WA.

Why the product was recalled

A shard of glass being found in one of the jars.

Distribution information

Distributed in IA, IL, IN, MI, MO, TN, and WI.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.

Related recall records

Other records from the same recalling company are shown first when available.