FDA Recall United States TerminatedTerminated: October 9, 2018Historical recordClass II
MUNK PACK INC
- Product
- Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz…
- Published
- May 16, 2018
- Distribution
- CA,CO,CT,FL,GA,IA,IL,IN,MA,MD,MS,NH,NJ,N…
MUNK PACK INC Recall: Mold growth on product. - F-1396-2018
United States
TerminatedClass II
- Company
- MUNK PACK INC
- Product
- Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT…
- Recall date
- February 21, 2018
- Terminated
- October 9, 2018
- Source
- FDA
Reason for recall
Mold growth on product.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT 2.96oz (84g); UPC: 853787005351 | 853787005351 | 1774 master cases (total for all products) | Lot # NOV022018, NOV012018, SEP25,2018 |
Distribution
- CA
- CO
- CT
- FL
- GA
- IA
- IL
- IN
- MA
- MD
- MS
- NH
- NJ
- NY
- NV
- OH
- OK.OR
- PA
- SC
- TX
- WA
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1396-2018
- Event ID
- 79934
- Status
- Terminated
- Classification
- Class II
- Company
- MUNK PACK INC
- Product description
- Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT 2.96oz (84g); UPC: 853787005351
- Quantity
- 1774 master cases (total for all products)
- Reason
- Mold growth on product.
- Recall initiation date
- February 21, 2018
- Report date
- May 16, 2018
- Classification date
- Not published in this source record
- Termination date
- October 9, 2018
- Distribution pattern
- CA,CO,CT,FL,GA,IA,IL,IN,MA,MD,MS,NH,NJ,NY,NV,OH,OK.OR,PA,SC,TX,WA,WI
- UPC, lot, and code information
- UPC 853787005351; Lot # NOV022018, NOV012018, SEP25,2018
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 79934 with 1 other product entry in Public Health Trace.
Responsible company: MUNK PACK INC
Other recalls from MUNK PACK INC
FDA Recall United States TerminatedTerminated: July 29, 2020Historical recordClass II
MUNK PACK INC
- Product
- Munk Pack Almond Butter Cocoa Chip Keto Granola Bar, 4 pack,…
- Published
- February 12, 2020
- Distribution
- NY and FL
FDA Recall United States TerminatedTerminated: July 29, 2020Historical recordClass II
MUNK PACK INC
- Product
- Munk Pack Coconut Cocoa Chip Keto Granola Bar, 4 pack, 128 g
- Published
- February 12, 2020
- Distribution
- NY and FL
FDA Recall United States TerminatedTerminated: July 29, 2020Historical recordClass II
MUNK PACK INC
- Product
- Munk Pack Peanut Butter Dark Chocolate Nut & Seed Bar, 35 g,…
- Published
- February 12, 2020
- Distribution
- NY and FL
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 |
|---|---|
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Mississippi | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New York | 1 |
| Nevada | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Texas | 1 |
| Washington | 1 |
| Wisconsin | 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 October 9, 2018.
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.
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.