Recall record at a glance
| Official record | F-0622-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Shearer's Foods, LLC |
| Report date | Mar 19, 2025 |
| Recall initiation date | Feb 21, 2025 |
| Quantity | 1.) 3330 cases; 2.) 9720 cases; 3.) 990 cases; 4.) 1440 cases; 5.) 394 cases; 15874 cases TOTAL |
| Location | Massillon, OH, United States |
Official product description
1.) Market Pantry Soup & Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case, Distributed By: Target Corporation, Minneapolis, MN 55403 2.) Great Value Soup & Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case, Distributed By: Walmart, Inc., Bentonville, AR 72716 3.) Giant Eagle Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case, Distributed By: Giant Eagle, Inc., Pittsburgh, PA 15238 4.) VISTA Soup & Oyster Crackers, NET WT 12 OZ (340g), packaged in flexible plastic bags, 12 count per case, Manufactured By: Shearer's Foods LLC, 100 Lincoln Way East, Massillon, OH 44646 5.) 20lb. Bulk Oyster Crackers, NET WT. 20 LBS., packaged in 20 lb. bulk bag-in-box (not for sale at retail)
Why the product was recalled
Potential foreign material (stainless steel wire)
Distribution information
Product distributed to customers in the following states: AL, CA, CO, FL, GA, IL, IN, KS, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, TX, VA, WA, and WI.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.