← FDA ENFORCEMENT
F-0734-2025Class II

S Martinelli & Company

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
S Martinelli & Company
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-04-30
Distribution
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
Firm state
CA
Product quantity
7234 cases
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential contamination with patulin.

Product description

Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack; 6 packs per case)

Code / lot info

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, 0001255024, 0001255010, 0001255002, 0001254862, 0001255013, 0001254979, 0001254980, 0001255029, 0001254875, 0001254906, 0001254915, 0001255032, 0001255003, 0001254981, 0001255029, 0001254874, 0001255000, 0001254944, 0001255021, 0001255022, 0001254866, 0001254977, 0001254871, 0001254999, 0001254865, 0001255031, 0001255025, 0001254997, 0001254916, 0001254922, 0001254985

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →