FDA recall record

Nanosphere Verigene BC-GP Kit recall — FDA Z-2735-2014

There is a specific Extraction Tray lot containing Tips that may slightly increase the occurrence of Process SP Processing Error when used due to the…

Class IIclassification
Z-2735-2014official record ID
Oct 8, 2014report date

Recall record at a glance

Official recordZ-2735-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNanosphere, Inc.
Report dateOct 8, 2014
Recall initiation dateJun 17, 2013
Quantity1,660 extraction trays
LocationNorthbrook, IL, United States

Official product description

Verigene BC-GP Kit (Catalog number 20-005-018); 1) 20 Verigene BC-GP Test Cartridges; are qualitative multiplexed in vitro diagnostic tests for simultaneous detection and identification of selected gram-positive (BC-GP) and gram-negative (BC-GN) bacteria and resistance markers.

Why the product was recalled

There is a specific Extraction Tray lot containing Tips that may slightly increase the occurrence of Process SP Processing Error when used due to the Processor SP experiencing difficulty releasing the Tip to the final location in the Tip Assembly. The difficult releasing the Tip can result in a Processing Error and occasionally the Tip to be dropped into the Processor SP.

Distribution information

Worldwide Distribution:US (Nationwide) including states of: AZ, CA, FL, IL, KY, MD, MN, MT, OH, PA, TN, TX, VA, WA, WI; and countries of: Belgium, China, and Saudi Arabia.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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Related recall records

Other records from the same recalling company are shown first when available.

Medical DeviceOct 8, 2014

Nanosphere Verigene BC-GN Kit recall — FDA Z-2736-2014

There is a specific Extraction Tray lot containing Tips that may slightly increase the occurrence of Process SP Processing Error when used due to the Processor SP experiencing difficulty…

Class IIFDA: TerminatedNanosphere, Inc.