Is KETOCONAZOLE, 200 MG, TABLET, Distributed by AidaPak Services LLC, NDC 00093-0900-01, 51672-4026-06. recalled?

Medium RiskFDA Drug

Aidapak Services, LLC: Penicillin Cross Contamination; There is potential for beta-lactam cross contamination of non-penicillin drug products repackaged in the same facility; There is a potential for Penicillin cross contamination.; Penicillin Cross Contamination; There is potential for beta-lactam cross contamination of non-penicillin drug products repackaged in the same facility.

Agency Publication Date: October 6, 2011

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 59173

Status: Resolved

Manufacturer: Aidapak Services, LLC

Manufactured In: United States

Units Affected: 179 products (130 TABLETS; 100 TABLETS; 300 tablets; 359 TABLETS; 240 Caplets; 14,444 Tablets; 400 Captabs; 11,272 Tablets; 2,698 Capsules; 12,394 Tablet; 1,072 Tablets; 237 Tablets; 2,194 Tablets; 1,316 Tablets; 3,353 Tablets; 2,200 Tablets; 100 Tablets; 30 Tablets; 30 TABLETS; 70 Tablets; 4,315 Tablets; 2,204 capsules; 90 TABLETS; 561 Tablets; 25 Tablets; 118 Tablets; 2,990 cups; 1,894 TABLETS; 6,252 Tablets; 597 Tablets; 60 Tablets; 150 Tablets; 100 Tablets; 4,272 Tablets; 6,792 tablets; 2300 Tablets; 1,398 tablets; 100 tablets; 1,495 Tablets; 2,099 Tablets; 2,195 Tablets; 1,093 tablets; 4,282 Tablets; 99 tablets; 1,000 Tablets; 500 tablets; 5850 syringes; 1,094 tablets; 530 tablets; 498 capsules; 500 capsules; 10,896 Tablets; 14,181 Tablets; 16,394 Tablets; 1650 tablets; 300 Tablets; 1550 tablets; 400 capsules; 8,383 capsules; 6,879 tablets; 4,398 capsules; 239 tablets; 13,932 tablets; 120 cups; 600 tablets; 4200 tablets; 25 syringes; 218 syringes; 179 Tablets; 8,446 Tablets; 6,599 tablets; 150 tablets; 199 tablets; 199 Capsules; 100 capsules; 1,494 capsules; 598 capsules; 4,311 tablets; 1,075 Tablets; 450 cups; 360 tablets; 100 Tablets; 403 syringes; 1,397 Tablets; 1597 tablets; 100 capsules; 2,695 Tablets; 2,796 Tablets; 299 tablets; 200 tablets; 100 tablets; 4,050 cups; 5,925 cups; 1,482 tablets; 11,291 Tablets; 99 tablets; 50 tablets; 120 tablets; 360 cups; 96 lozenges; 135 Tablets; 910 Capsules; 17,440 Tablets; 1,498 tablets; 700 tablets; 10,152 tablets; 7,099 tablets; 417 Tablets; 100 tablets; 11,071 tablets; 100 tablets; 99 tablets; 297 tablets; 1,197 tablets; 600 tablets; 299 tablets; 99 tablets; 599 capsules; 99 tablets; 695 tablets; 100 tablets; 421 tablets; 473 syringes; 100 tablets; 100 tablets; 200 tablets; 300 tablets; 2,297 tablets; 299 tablets; 3,195 tablets; 4,989 tablets; 8,196 tablets; 7,242 tablets; 200 capsules; 99 capsules; 499 capsules; 239 tablets; 21,945 syringes; 1,898 tablets; 1,196 tablets; 699 tablets; 200 tablets; 50 capsules; 300 capsules; 299 tablets; 898 tablets; 357 tablets; 924 tablets; 1,040 tablets; 1,479 tablets; 60 tablets; 100 tablets; 100 tablets; 210 tablets; 58 tablets; 150 tablets; 30 tablets; 269 tablets; 1,000 dose packs; 5,828 tablets; 900 tablets; 60 tablets; 200 tablets; 225 cups; 465 dose packs; 239 tablets; 3455 cups; 6,156 tablets; 60 tablets; 1000 tablets; 2,892 tablets; 1,199 tablets; 4,677 tablets; 17237 cups; 12,284 capsules; 2,998 tablets; 1,798 tablets; 599 tablets; 500 capsules)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.