Laduree Usa Recall: Imported Frozen Poppy Seed bread contains elevated levels of Morphine and Codeine.
United States
TerminatedClass II
- Company
- Laduree Usa
- Product
- Frozen Poppy Seed Bread (57 grams), UPC Codes: (01)035564200…
- Recall date
- April 8, 2019
- Terminated
- July 15, 2019
- Source
- FDA
Reason for recall
Imported Frozen Poppy Seed bread contains elevated levels of Morphine and Codeine.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Frozen Poppy Seed Bread (57 grams), UPC Codes: (01)03556420003673(15)191122(10)181122(91)0937326, Lot 22112018 | Not published in this source record | 51.5 cases consumed, 128.5 cases still in firm possesion (120 pieces of Bread in Each) | Manufacturer Lot Codes: 06102018 & 22112018, Consignee Assigned Lot Codes 09023E & 090063E |
Distribution
- Product was distributed from a NJ warehouse to 2 CA warehouses and Restaurants in Washington DC and NY. Firm states affected product was not further distributed to any California Restaurants
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1331-2019
- Event ID
- 82591
- Status
- Terminated
- Classification
- Class II
- Company
- Laduree Usa
- Product description
- Frozen Poppy Seed Bread (57 grams), UPC Codes: (01)03556420003673(15)191122(10)181122(91)0937326, Lot 22112018
- Quantity
- 51.5 cases consumed, 128.5 cases still in firm possesion (120 pieces of Bread in Each)
- Reason
- Imported Frozen Poppy Seed bread contains elevated levels of Morphine and Codeine.
- Recall initiation date
- April 8, 2019
- Report date
- May 15, 2019
- Classification date
- Not published in this source record
- Termination date
- July 15, 2019
- Distribution pattern
- Product was distributed from a NJ warehouse to 2 CA warehouses and Restaurants in Washington DC and NY. Firm states affected product was not further distributed to any California Restaurants
- UPC, lot, and code information
- Manufacturer Lot Codes: 06102018 & 22112018, Consignee Assigned Lot Codes 09023E & 090063E
- 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: Laduree Usa
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 |
|---|---|
| New Jersey | 1 |
| California | 1 |
| District of Columbia | 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:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
