Maryland Packaging, LTD. Recall: Possible foreign object: metal wire - F-0831-2020
United States
TerminatedClass II
- Company
- Maryland Packaging, LTD.
- Product
- Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper…
- Recall date
- February 27, 2020
- Terminated
- June 11, 2020
- Source
- FDA
Reason for recall
Possible foreign object: metal wire
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper bags on 2 1/2 CHEP pallets | Not published in this source record | 4056 bags | M0071A7 and M0071B7 |
Distribution
- The product was distributed to PA and MD
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0831-2020
- Event ID
- 85160
- Status
- Terminated
- Classification
- Class II
- Company
- Maryland Packaging, LTD.
- Product description
- Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper bags on 2 1/2 CHEP pallets
- Quantity
- 4056 bags
- Reason
- Possible foreign object: metal wire
- Recall initiation date
- February 27, 2020
- Report date
- March 18, 2020
- Classification date
- Not published in this source record
- Termination date
- June 11, 2020
- Distribution pattern
- The product was distributed to PA and MD
- UPC, lot, and code information
- M0071A7 and M0071B7
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Maryland Packaging, LTD.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Pennsylvania | 1 |
| Maryland | 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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of June 11, 2020.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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