Drug recall

Osceola Perineal Solution with Aloe Vera 8 fl. oz. bottle. Lot # 45-11239C

FDA recall event 56095 · Class II · Canberra Corporation

Key facts

Event ID 56095
Recall numbers F-2650-2010
Recalling firm Canberra Corporation
Product type Food
Products Osceola Perineal Solution with Aloe Vera 8 fl. oz. bottle. Lot # 45-11239C
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall The firm received a complaint from a customer indicating that the product may be contaminated with Pseudomonas putida. The firm tested retain samples of the product and the results was positive for…
Initiation date Jun 7, 2010
Termination date Oct 15, 2010
City Toledo
State OH
Country United States
FEI number 1000508133

At a glance

  • 1–9 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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