Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1717-2018Class II

BEQ-TOP 49101 Childrens Large ECC Pack, Custom Tubing Kit, Catalog No. 701067069R01

Datascope Corp. / initiated 2017-10-19 / Terminated / root cause: manufacturing process

Datascope Corporation began a recall of BEQ-TOP 49101 Childrens Large ECC Pack, Custom Tubing Kit, Catalog No. 701067069R01 on . FDA classified it as Class II and gives the reason as "The Better Bladder device provided as part of some custom tubing kits has been recalled by its manufacturer. Seal separation from the housing may allow air to enter the housing and collapse the balloon. This may...". As of , the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-1717-2018
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Datascope Corp.
Product
BEQ-TOP 49101 Childrens Large ECC Pack, Custom Tubing Kit, Catalog No. 701067069R01
Product code
DWE Tubing, Pump, Cardiopulmonary Bypass
Reason for recall
The Better Bladder device provided as part of some custom tubing kits has been recalled by its manufacturer. Seal separation from the housing may allow air to enter the housing and collapse the balloon. This may increase resistance to flow in the venous line and cause a drop in ECMO circuit blood flow.
Root cause tag
manufacturing process
FDA root cause
Process control
Action
Affected consignees were notified by letter delivered via FedEx on October 19, 2017. After CTI expanded their recall in March 2018, Getinge accordingly alerted additionally affected consignees by letter delivered via FedEx on April 5, 2018. The recall letter advised customers of the issue and referenced the CTI recall notification, which was included as an attachment to Getinge's communication. End-users were instructed to examine their inventory to determine if they had any of the affected catalog/lot numbers. Any affected product is to be immediately quarantined and returned to Getinge by contacting Customer Service at 1(888) 627-8383 (option 2, then option 2 again), Monday through Friday, 8AM-6PM. In addition, customers were asked to complete a response form to acknowledge receipt of the notification, and return to Getinge. After communications with some end-users who were concerned about maintaining inventory of custom tubing kits, Getinge revised their recall strategy to include an option for replacement of the recalled Better Bladder device. Customers who wished to receive a replacement device will be provided with the device and a notice which must be affixed to the recalled kit. This will ensure that at time of use, it will be obvious to the user that the Better Bladder device inside the kit must be switched out with the replacement device prior to use. The removed recalled Better Bladder device must then be sent back to the recalling firm, Getinge. This information was communicated to customers via telephone call or visit on 4/20/18, and a summary of the communication was sent as an amended recall notification to customers who stated during the phone call that they still had recalled product on 4/21/18. Maquet/Getinge Customer support may be reached at 1(888) 627-8383 (press option 2, then option 2), Monday through Friday, 8AM-6PM.
Quantity in commerce
4
Distribution
Distributed to accounts in AL, AR, CA, DC, FL, IL, LA, MO, NC, PA, SC, TX, and WA.
Product codes and lots
Lot 3000059724

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1717-2018
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1706-2018Class IITerminatedVoluntary: Firm initiated
Z-1707-2018Class IITerminatedVoluntary: Firm initiated
Z-1708-2018Class IITerminatedVoluntary: Firm initiated
Z-1709-2018Class IITerminatedVoluntary: Firm initiated
Z-1710-2018Class IITerminatedVoluntary: Firm initiated
Z-1711-2018Class IITerminatedVoluntary: Firm initiated
Z-1712-2018Class IITerminatedVoluntary: Firm initiated
Z-1713-2018Class IITerminatedVoluntary: Firm initiated
Z-1714-2018Class IITerminatedVoluntary: Firm initiated
Z-1715-2018Class IITerminatedVoluntary: Firm initiated
Z-1716-2018Class IITerminatedVoluntary: Firm initiated
Z-1717-2018Class IITerminatedVoluntary: Firm initiated
Z-1718-2018Class IITerminatedVoluntary: Firm initiated
Z-1719-2018Class IITerminatedVoluntary: Firm initiated
Z-1720-2018Class IITerminatedVoluntary: Firm initiated
Z-1721-2018Class IITerminatedVoluntary: Firm initiated
Z-1722-2018Class IITerminatedVoluntary: Firm initiated
Z-1723-2018Class IITerminatedVoluntary: Firm initiated
Z-1724-2018Class IITerminatedVoluntary: Firm initiated
Z-1725-2018Class IITerminatedVoluntary: Firm initiated
Z-1726-2018Class IITerminatedVoluntary: Firm initiated
Z-1727-2018Class IITerminatedVoluntary: Firm initiated
Z-1728-2018Class IITerminatedVoluntary: Firm initiated
Z-1729-2018Class IITerminatedVoluntary: Firm initiated
Z-1730-2018Class IITerminatedVoluntary: Firm initiated
Z-1731-2018Class IITerminatedVoluntary: Firm initiated
Z-1732-2018Class IITerminatedVoluntary: Firm initiated
Z-1733-2018Class IITerminatedVoluntary: Firm initiated