🔍 RecallPedia

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7852-01; NDC Berkley Jensen: 68391-852-56; NDC: CVS Health: 59779-540-01; NDC DG Health: 55910-011-01; NDC Kirkland: 63981-852-56; NDC Kroger: 30142-600-56; NDC Meijer: 41250-852-01; NDC Rite Aid: 11822-0852-4; NDC Walgreens: 0363-0852-01

Class I - Dangerous
💊 Drugs Recalled: October 23, 2019 Perrigo Company PLC Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lots:8CE1446, 8DE1740, 8FE1238, 8FE1794, 8GE1964, 8JE2159, 8ME2546, 8ME2547, 9BE3011, 9CE3854, 9DE3158, 9FE3340, 9HE3445, 9JE2663, 8AE1779, 8BE1414, 8DE1199, 8DE1200, 8DE1532, 8EE1321, 8FE1239, 8FE1346, 8FE1793, 8HE1516, 8KE2563, 8KE2563R, 8LE2260, 9AE2610, 9AE2612, 9BE3012, 9BE3013, 9CE3852, 9DE3156R, 9DE3160, 9DE3161, 9EE2952, 9FE3338, 9GE2993, 8AV1095, 8AV1150, 8AV1235, 8AV1236, 8AV1237, 8BV0896, 8BV0897, 8BV0910, 8BV1737, 8BV1757, 8BV1758, 8CV0930, 8CV1316, 8CV1317, 8CV1319, 8CV1324, 8CV1633, 8DV1128, 8DV1129, 8DV1134, 8EV0993, 8EV0994, 8EV0995, 8EV1240, 8FV0712, 8FV0912, 8FV0913, 8FV0914, 8FV0915, 8GV0847, 8GV0849, 8GV0997, 8HV0926, 8HV0928, 8HV1534, 8HV1535, 8JV0730, 8JV0944, 8KV2339, 8KV2348, 8KV2485, 8LV1791, 8LV2205, 8MV1650, 8MV1712, 9AV2395, 9AV2679, 9AV2680, 9BV2182, 9CV1345, 9CV1346, 9CV1347, 9CV1348, 9CV1349, 9DV1511, 9DV1515, 9EV1422, 9EV1585, 9EV1596, 9FV1132, 9FV1275R, 9FV1330, 9FV1331, 9FV1332, 9FV1333, 9FV1339, 9FV1954, 9FV1972, 9GV1675, 9GV1994, 9HV1415
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Perrigo Company PLC
Reason for Recall:
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7852-01; NDC Berkley Jensen: 68391-852-56; NDC: CVS Health: 59779-540-01; NDC DG Health: 55910-011-01; NDC Kirkland: 63981-852-56; NDC Kroger: 30142-600-56; NDC Meijer: 41250-852-01; NDC Rite Aid: 11822-0852-4; NDC Walgreens: 0363-0852-01

Product Codes/Lot Numbers:

Lots:8CE1446, 8DE1740, 8FE1238, 8FE1794, 8GE1964, 8JE2159, 8ME2546, 8ME2547, 9BE3011, 9CE3854, 9DE3158, 9FE3340, 9HE3445, 9JE2663, 8AE1779, 8BE1414, 8DE1199, 8DE1200, 8DE1532, 8EE1321, 8FE1239, 8FE1346, 8FE1793, 8HE1516, 8KE2563, 8KE2563R, 8LE2260, 9AE2610, 9AE2612, 9BE3012, 9BE3013, 9CE3852, 9DE3156R, 9DE3160, 9DE3161, 9EE2952, 9FE3338, 9GE2993, 8AV1095, 8AV1150, 8AV1235, 8AV1236, 8AV1237, 8BV0896, 8BV0897, 8BV0910, 8BV1737, 8BV1757, 8BV1758, 8CV0930, 8CV1316, 8CV1317, 8CV1319, 8CV1324, 8CV1633, 8DV1128, 8DV1129, 8DV1134, 8EV0993, 8EV0994, 8EV0995, 8EV1240, 8FV0712, 8FV0912, 8FV0913, 8FV0914, 8FV0915, 8GV0847, 8GV0849, 8GV0997, 8HV0926, 8HV0928, 8HV1534, 8HV1535, 8JV0730, 8JV0944, 8KV2339, 8KV2348, 8KV2485, 8LV1791, 8LV2205, 8MV1650, 8MV1712, 9AV2395, 9AV2679, 9AV2680, 9BV2182, 9CV1345, 9CV1346, 9CV1347, 9CV1348, 9CV1349, 9DV1511, 9DV1515, 9EV1422, 9EV1585, 9EV1596, 9FV1132, 9FV1275R, 9FV1330, 9FV1331, 9FV1332, 9FV1333, 9FV1339, 9FV1954, 9FV1972, 9GV1675, 9GV1994, 9HV1415

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1026-2020

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