Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack... — FDA record F-0734-2025

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 18, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

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)
Reason
Potential contamination with patulin.
Classification
Class II
Recalling firm
S Martinelli & Company
Quantity
7234 cases
Agency-reported status
Terminated
Source record identifier
F-0734-2025

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUPC: 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

Match all identifying details in the current notice. A brand name alone is not enough.

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Apr 30, 2025
Recall initiation date
Mar 18, 2025
Center classification date
Apr 22, 2025
Termination date
Jul 14, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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