Class IITerminatedVoluntary: Firm initiated
S Martinelli & Company: food recall F-0734-2025
S Martinelli & Company of Watsonville, CA recalled Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack;… Reason: Potential contamination with patulin. The FDA listed it as Class II in its Enforcement Report dated Apr 30, 2025; distribution: Alabama, Arkansas, Arizona, California, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Missouri, Mississippi, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, South Carolina, Texas, Utah, Virginia, Wisconsin.
Record status as published: Terminated (terminated Jul 14, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack; 6 packs per case)
- Product quantity
- 7234 cases
- Reason for recall
- Potential contamination with patulin.
- Codes, lots and dates on the package
- UPC: 0 41244 64102 2 BEST BY: 05DEC2026 Pallet/Batch Numbers: 0001254859, 0001255023, 0001255026, 0001254864, 0001254917, 0001254874, 0001254984, 0001254860, 0001255030, 0001255033, 0001254901, 0001254913, 0001254884, 0001254903, 0001254857, 0001255027, 0001254861, 0001254924, 0001254957, 0001254876, 0001255001, 0001254856, 0001255020, 0001254863, 0001254909, 0001254914, 0001254873, 0001254878, 0001255009, 0001254996, 0001254987, 0001254902, 0001254972, 0001254922, 0001254872, 0001255011, 0001254993, 0001254998, 0001254921, 0001254910, 0001255015, 0001254870, 0001255028, 0001254897, 0001254983, 0001254892, 0001254919, 0001254925, 0001254887, 0001255014, 0001255016, 0001254992, 0001254920, 0001254922, 0001255005, 0001254899, 0001254923, 0001254867, 0001254982, 0001255006, 0001254978, 0001254951, 0001254877, 0001254907, 0001255019, 0001254990, 0001254888, 0001254918, 0001254954, 0001254926, 0001254885, 0001254869, 0001254991, 0001254890, 0001255012, 0001254927, 0001254868, 0001254883, 0001255008, 0001254994, 0001254905, 0001255018, 0001255004, 0001254939, 0001254881, 0001254858, 0001254989, 0001255005, 0001254882, 0001254929, 0001254953, 0001255017, 0001254986, 0001254995,…
- Distribution pattern
- AL, AR, AZ, CA, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MO, MS, NC, NH, NJ, NY, OH, PA, SC, TX, UT, VA, WI
- Recalling firm
- S Martinelli & Company, Watsonville, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 18, 2025 |
| Classified by the FDA | Apr 22, 2025 |
| Published in the Enforcement Report | Apr 30, 2025 |
| Terminated | Jul 14, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0734-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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