Pacific Coast Producers recalls diced Bartlett pears in extra light syrup due to potential foreign object contamination. Consumers should check product codes and contact the company for details.
“Pacific Coast Producers Diced Pears Recall: Foreign Object Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/8483-pacific-coast-producers-diced-pears-recall-foreign-object-contamination-risk. Based on FDA recall #F-0432-2025 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0432-2025%22&limit=1).
The FDA announced on Dec. 5, 2024, that Pacific Coast Producers voluntarily recalled Diced Bartlett Pears In Extra Light Syrup due to potential foreign object contamination. The recall affects products distributed in Kentucky, Michigan, Ohio, and Pennsylvania.
How to tell if you have it
Brand: Pacific Coast Producers
Product: Diced Bartlett Pears In Extra Light Syrup
Size: 105 OZ (6 LB 9 OZ)
Packaging: Metal can, hermetically sealed
Lot code: 6PDL 05 A2644
Distribution: KY, MI, OH, PA
The hazard
The product poses a potential contamination hazard with foreign objects. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Pacific Coast Producers has two other recalls on record since Nov. 30, 2020. Other recent recalls of similar products include Dakota Honey Spreadable Spun Honey Recall (April 4, 2026), Gifford's POWER PLAY FUDGE Ice Cream Recall (Aug. 14, 2026), and Dakota Honey Spreadable Spun Honey Jalapeno Recall (April 4, 2026).
How to tell if you have this one
Check for the product code 6PDL 05 A2644 on the metal can packaging. The product is sold in 105 oz (6 lb 9 oz) containers with hermetically sealed metal cans.
Brand
Pacific Coast Producers
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Code
Look for the product code 6PDL 05 A2644 on the metal can packaging.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “KY, MI, OH, PA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Kentucky, Michigan, Ohio, Pennsylvania.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0432-2025 (December 5, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0432-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.