Drug recall

Nabumetone, 500 MG, TABLET, Distributed by: AidaPak Service, LLC, NDC 00185-0145-01.

FDA recall event 59237 · Class II · Aidapak Services, LLC

Key facts

Event ID 59237
Recall numbers D-002-2012, D-003-2012, D-004-2012, D-005-2012, D-006-2012, D-007-2012, D-008-2012, D-009-2012, D-010-2012, D-011-2012, D-012-2012, D-013-2012 and 209 more
Recalling firm Aidapak Services, LLC
Product type Drugs
Products Nabumetone, 500 MG, TABLET, Distributed by: AidaPak Service, LLC, NDC 00185-0145-01., Nabumetone, 750 MG, TABLET, Distributed by: AidaPak Service, LLC, a) NDC 00185-0146-01, b) NDC 68462-0359-01., N-Acetyl-Cysteine, 600 MG, CAPSULE, Distributed by: AidaPak Service, LLC, NDC 27434-0002-11., Nadolol, 20 MG, TABLET, Distributed by: AidaPak Service, LLC, a) NDC 00093-4235-01, b) NDC 00781-1181-01., Nadolol, 40 MG, TABLET, Distributed by: AidaPak Service, LLC, NDC 00781-1182-01. and 216 more
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Penicillin Cross Contamination: There is potential for beta-lactam cross contamination of non-penicillin drug products repackaged in the same facility, Penicillin Cross Contamination: There is potential for beta-lactam cross contamination of non-penicillin drug products repackaged in the same facility., Penicillin Cross Contamination; There is potential for beta-lactam cross contamination of…
Initiation date May 19, 2011
Termination date Apr 18, 2012
City Vancouver
State WA
Country United States
FEI number 3008673824

At a glance

  • 100–999 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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