Recalls / Class I
Class IF-1829-2017
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Premo Asiago Italian Item # 207919, Net Wt 6 oz; Fresh Grab Asiago Italian Item # 251847, Net Wt 6 oz; Core-Mark Asiago Italian Item # 568377, Net Wt 6 oz;
- Type
- Food
- Affected lot / code info
- Item #: 207919, Lot #s: 05201701, 06201701, 09201701, 10201701, 11201701, 13201701, 16201701, 18201701, Best By 1/26/17 to 2/8/17; Item # 251847, Lot #s: 025201701, 06201701, 10201701, 17201701, Best By: 1/26/17 to 2/7/17; Item # 568377, Lot #s: 06201701 and 13201701, Best By: 1/26/17 and 1/27/17
- Quantity
- 8695 sandwiches
Why it was recalled
JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
Recalling firm
- Firm
- Lipari Foods, Inc.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 26661 Bunert Rd, N/A, Warren, Michigan 48089-3650
Distribution
- Distribution pattern
- Domestic: MI, IL, IN, KY, MD, OH, PA, TN, VA, WI, WV Foreign: None VA/DOD: None
Timeline
- Recall initiated
- 2017-02-21
- FDA classified
- 2017-04-03
- Posted by FDA
- 2017-04-12
- Terminated
- 2017-07-18
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1829-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.