Laubscher Cheese Co.; Shredded Cheese; Net Wt. 5 LBS. and 2 LBS.,Cryovac sealed plastic bags, Distributed By: Laubscher Cheese Co. Mercer...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0601-2020.
Laubscher Cheese Company, LTD , has initiated a recall of Shredded Cheese, because samples of the shredded cheese were found positive for Listeria Monocytogenes
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0601-2020.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Laubscher Cheese Company, Ltd. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0601-2020.
Laubscher Cheese Company, Ltd.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Laubscher Cheese Company, Ltd. Recall FAQ
Laubscher Cheese Company, Ltd. is the subject of a dairy safety report: Laubscher Cheese Co.; Shredded Cheese; Net Wt. 5 LBS. and 2 LBS.,Cryovac sealed plastic bags, Distributed By: Laubscher Cheese Co. Mercer.... The notice was published on November 29, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 1,617,420 units are potentially affected.