CLASS II Food recall · Reported 15 May 2024 · FDA Enforcement Report
Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh recalled
S Martinelli & is recalling Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh Apples No Additives of Any Kind, distributed in 35 states. The recall was initiated on 16 Apr 2024 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1220-2024
- FDA event ID
- 94480
- Recalling firm
- S Martinelli &, Watsonville, CA
- Brand
- Martinelli's Gold
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 16 Apr 2024
- FDA classified
- 6 May 2024
- Reported
- 15 May 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Lead & Heavy Metals
- Product category
- Juice
Timeline
| 16 Apr 2024 | Recall initiated by company | |
| 6 May 2024 | Classified by FDA | +20 days |
| 15 May 2024 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Elevated levels of inorganic arsenic.
Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.
Product as listed by the FDA
Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh Apples 1 Liter (33.8 fl oz.) No Additives of Any Kind UPC 0 00 41244 00102 6
Where it was distributed
U.S. distribution to the following: AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, PR, SC, TN, TX, UT, VA, WA, WI Foreign distribution to the following: Panama
AlabamaArkansasArizonaCaliforniaColoradoFloridaGeorgiaIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMarylandMichiganMinnesotaMissouriMississippiNorth Carolina
Questions about this recall
Why was it recalled?
Elevated levels of inorganic arsenic.
Which lots are affected?
Best By 09MAR2026 and 10MAR2026 Production Date: 3/09/23 Pallet/Batch #: 0001058704, 0001058705, 0001058708, 0001058709, 0001058738, 0001058739, 0001058762, 0001058763, 0001058772, 0001058773, 0001058774, 0001058778, 0001058779, 0001058780, 0001058781, 0001058783, 0001058784, 0001058787, 0001058788, 0001058797, 0001058798, 0001058806, 0001058807, 0001058809, 0001058810, 0001058811, 0001058814, 0001058815, 0001058820, 0001058821, 0001058823, 0001058835, 0001058836, 0001058854, 0001058855, 0001058856, 0001058865, 0001058876, 0001058888, 0001058889, 0001058890, 0001058892, 0001058893, 0001058898, 0001058899, 0001058900, 0001058901, 0001058902, 0001058904, 0001058905, 0001058915, 0001058916, 0001058917, 0001058918, 0001058919, 0001058921, 0001058922, 0001058923, 0001058925, 0001058926, 0001058935, 0001058936, 0001058947, 0001058952, 0001058953, 0001058954, 0001058955, 0001058957, 0001058958, 0001058964, 0001058965, 0001058968, 0001058970, 0001058975, 0001058976, 0001058984, 0001058988, 0001058990, 0001059012, 0001059019, 0001059020, 0001059021, 0001059022, 0001059024, 0001059025, 0001059028, 0001059031, 0001059039, 0001059040, 0001059044, 0001059045 0001059046, 0001059053, 0001059054, 0001059060, 0001059065, 0001059071, 0001059077, 0001059078, 0001059082, 0001059094, 0001059096, 0001059097, 0001059100, 0001059104, 0001059118, 0001059137, 0001059144, 0001059149, 0001059158, 0001059163, 0001059167, 0001059168, 0001059170, 0001059179, 0001059181, 0001059185, 0001059186, 0001059187, 0001059204, 0001059207, 0001059210, 0001059212, 0001059213, 0001059217, 0001059225, 0001059226, 0001059228, 0001059230, 0001059236, 0001059237, 0001059238, 0001059243, 0001059244, 0001059247, 0001059249, 0001059250, 0001059252, 0001059255, 0001059257, 0001059262, 0001059266, 0001059267, 0001059269, 0001059275, 0001059276, 0001059277, 0001059279, 0001059281, 0001059285, 0001059287, 0001059297, 0001059298, 0001059299, 0001059300, 0001059301, 0001059302, 0001059303, 0001059307, 0001059310, 0001059311, 0001059314, 0001059316, 0001059323, 0001059326, 0001059327, 0001059332, 0001059333, 0001059334, 0001059335, 0001059336, 0001059337, 0001059339, 0001059340, 0001059346, 0001059347, 0001059348, 0001059350, 0001059356, 0001059358, 0001059360, 0001059362, 0001059369, 0001059371, 0001059372, 0001059376, 0001059378 Production Date: 3/10/23 Pallet/Batch #: 0001059388, 0001059396, 0001059399, 0001059400, 0001059403, 0001059404, 0001059406, 0001059407, 0001059409, 0001059411, 0001059412, 0001059421, 0001059424, 0001059425, 0001059426, 0001059427, 0001059428, 0001059429, 0001059430, 0001059431, 0001059432, 0001059433, 0001059439, 0001059440, 0001059441, 0001059442, 0001059443, 0001059444, 0001059459, 0001059470, 0001059477, 0001059478, 0001059481, 0001059482, 0001059485, 0001059488, 0001059489, 0001059491, 0001059492, 0001059494, 0001059499, 0001059501, 0001059503, 0001059504, 0001059505, 0001059506, 0001059507, 0001059508, 0001059509, 0001059512, 0001059515, 0001059520, 0001059522, 0001059524, 0001059526, 0001059528, 0001059530, 0001059531, 0001059532, 0001059533, 0001059534, 0001059536, 0001059537, 0001059539, 0001059540, 0001059541, 0001059542, 0001059543, 0001059544, 0001059545, 0001059546, 0001059547, 0001059550, 0001059551, 0001059554, 0001059558, 0001059562, 0001059565, 0001059566, 0001059567, 0001059571, 0001059575, 0001059578, 0001059583 0001059586, 0001059598, 0001059599
Where was it sold?
U.S. distribution to the following: AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, PR, SC, TN, TX, UT, VA, WA, WI Foreign distribution to the following: Panama
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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