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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87656

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 25, 2021
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Bard Peripheral Vascular Inc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829500, UDI: (01) 00801741027185 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.

Z-1550-2021
Recall number
Z-1550-2021
Initiated
March 25, 2021
Classification
Class II
Status
Terminated
Quantity
2,194 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

Code information

Code: REEU3063, REEV0989, REEV2633, REEX1380, REEZ1991

Distribution pattern

US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV.

device · product 2 of 3

PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829570, UDI: (01) 00801741027192 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.

Z-1551-2021
Recall number
Z-1551-2021
Initiated
March 25, 2021
Classification
Class II
Status
Terminated
Quantity
189 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

Code information

Code: REEW1060, REEX0568, REEZ1841

Distribution pattern

US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV.

device · product 3 of 3

PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 5829502, UDI: (01)00801741027406 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.

Z-1552-2021
Recall number
Z-1552-2021
Initiated
March 25, 2021
Classification
Class II
Status
Terminated
Quantity
287 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

Code information

Code: REEV2356, REEX1383, REEX3996

Distribution pattern

US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV.