Lidl US TRADING Recall: Container integrity issued (punctured lid)

🇺🇸 United States

1. January 25, 2024 - Recall initiated
2. March 20, 2024 - Reported by source
3. September 26, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1063-2024

Event ID

93914

Status

Terminated

Classification

Class III

Company

Lidl US TRADING

Product description

Banana Pepper Rings 16 FL OZ (1PT) 473ml UPC:4056489223863. Packaged in a glass jar with metal lid.

Quantity

23,904 jars

Reason

Container integrity issued (punctured lid)

Recall initiation date

January 25, 2024

Report date

March 20, 2024

Classification date

Not published in this source record

Termination date

September 26, 2024

Distribution pattern

Distributed to distribution centers and retails stores in MD, NC, VA, GA, SC, PA, NJ, NY and Washington D.C.

UPC, lot, and code information

UPC 4056489223863; Best before May/28/2026 L789/23 Best before Jul/28/2026 L1051

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Lidl US TRADING

Other recalls from Lidl US TRADING

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Maryland	1
North Carolina	1
Virginia	1
Georgia	1
South Carolina	1
Pennsylvania	1
New Jersey	1
New York	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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