Becton Dickinson Recalls BBL DrySlide Oxidase Kits Due to Packaging Error
Becton Dickinson is recalling BBL DrySlide Oxidase Kits because they were placed in incorrect packaging for distribution to laboratories.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a packaging error for a diagnostic aid without reported injuries, fitting the criteria for a moderate severity recall.
Plain-English summary
Becton Dickinson & Co. is recalling 610 BBL DrySlide Oxidase Kits, catalog number 231746, lot 2222008, with an expiration date of 08/31/13. The recall was initiated because the in-vitro diagnostic agents were placed into incorrect packaging for distribution.
The affected kits are used as a presumptive diagnostic aid for gram-negative bacteria. The product was distributed worldwide, including the United States, Australia, Canada, Europe, Hong Kong, Mexico, New Zealand, Singapore, and Taiwan.
Microbiological laboratories should stop using the affected kits and contact Becton Dickinson for instructions on return or disposal. No illnesses or injuries have been reported in connection with this recall.
The recalled product
- Product
- BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.
- Manufacturer
- Becton Dickinson & Co.
- Affected units
- 610
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Oxidase kit - lot 2222008 with expiration date 08/31/13
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Becton Dickinson & Co. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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