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Recall Observatory FDA recall evidence

Device product

Brand Name: Basal/Bolus Infusor. Indicated for the intravenous administration of medications.

Z-1606-2013

June 07, 2013

Class II

Product summary

Firm
Baxter Healthcare Corp.
Event
Event 65365
Status
Terminated
Classification
Class II
Quantity
3,255,096 total
Official record key
device-enforcement:Z-1606-2013

Official wording

Reason: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process improvements which have substantially improved product quality. Complaint rates for ruptures have since decreased. Baxter wants to ensure that no affected product remains in the field.

Code information: Product Codes: 2C1955KJP, 2C1976KJ Lot Codes: 08K006 08M038 08N001 09C021 09E028 09F078 09H080 09J046 09M052 09N030 09N048 10A043 108023 10E054 10H055 10J031 10K050 10M085 10N026 09H033 10B028 10B081 10E004 10J106 Expiration Dates: 06/30/15, 12/31/14, 12/31/15, 06/30/14, 12/31/14

Distribution pattern: Distributed Nationwide and in Puerto Rico.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process improvements which have substantially improved product quality. Complaint rates for ruptures have since decreased. Baxter wants to ensure that no affected product remains in the field.