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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81417

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
October 05, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Covidien LLC

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.

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Complete imported group

Every recalled product in this event

1 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 1

Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20) Product Usage: The PCOPM15 and PCOPM20 reorder codes are circular in shape, made from a three-dimensional monofilament polyester fabric with a two-dimensional monofilament polyester central band. One side of the design is completely covered with the hydrophilic film. On the opposite side, only the two-dimensional central band is coated with the absorbable hydrophilic film. The film extends 5 mm over the external edge of the reinforcement. The Parietex composite parastomal mesh is indicated for the reinforcement of soft tissues during surgical repair, and specifically for the repair of parastomal hernias. The non-absorbable polyester mesh provides long term reinforcement of soft tissues. The absorbable hydrophilic film minimizes tissue attachment to the mesh when in direct contact with the viscera.

Z-0461-2019
Recall number
Z-0461-2019
Initiated
October 05, 2018
Classification
Class II
Status
Terminated
Recalling firm
Covidien LLC
Quantity
7333

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm is issuing this voluntary removal following receipt of reports of parastomal mesh failure identified several years following parastomal hernia repair using the modified Sugarbaker repair technique. In these reports, product failure led to hernia recurrence requiring additional surgical treatment. Symptoms of hernia recurrence may include discomfort, localized pain-free or painful bulging, and possible changes in the overlying skin. Medtronic has received, worldwide, a total of ten reports of mesh failure following use of the product in the last five years. Patients who have received a Parietex" composite parastomal mesh for the treatment of a parastomal hernia should continue to receive ongoing monitoring by their healthcare providers for the recurrence of a parastomal hernia.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

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Inspect official wording and provenance

Reason for recall

The firm is issuing this voluntary removal following receipt of reports of parastomal mesh failure identified several years following parastomal hernia repair using the modified Sugarbaker repair technique. In these reports, product failure led to hernia recurrence requiring additional surgical treatment. Symptoms of hernia recurrence may include discomfort, localized pain-free or painful bulging, and possible changes in the overlying skin. Medtronic has received, worldwide, a total of ten reports of mesh failure following use of the product in the last five years. Patients who have received a Parietex" composite parastomal mesh for the treatment of a parastomal hernia should continue to receive ongoing monitoring by their healthcare providers for the recurrence of a parastomal hernia.

Code information

Lots PNI0064 PNI0065 PNI0402 PNJ0496 PNJ0989 PNJ0990 PNK0641 PNL0037 PNL0039 PNL0631 POA0469X POA0963X POB0030X POB0797X POC0036X POC0726X POD0033X POD0036X POD1016X POE0149X POE0262X POE0727X POF0295X POF0298X POG0047X POH0069X POH0070X POI0260X POI0261X POI0489X POJ0418X POJ0880X POK0364X POK0366X POK0789X POK0790X POL0082X PPA0226X PPA0227X PPA0508X PPA0509X PPB0779X PPB0780X PPC0578X PPD0409X PPD0410X PPE0215X PPE0509X PPF0179X PPF0181X PPF0836X PPG0035X PPG0723X PPH0355X PPI0630X PPI0631X PPI1144X PPI1145X PPJ0234X PPJ0235X PPJ0698X PPK0523X PPK0524X PPL0082X PPL0353X PQA0483X PQC0100X PQC0102X PQD0395X PQD0397X PQE0187X PQE0802X PQG0391X PQG1150X PQG1152X PQH0608X PQH0610X PQI1246X PQI1248X PQJ0971X PQJ0973X PQK0314X PQK0316X PQL0150X PQL0479X PQL0481X PRA1193X PRA1195X PRA1655X PRA1657X PRA2444X PRA2446X PRB1650X PRB1652X PRB2015X PRB2017X PRC0392X PRC0394X PRC1062X PRC1064X PRD0248X PRD0250X PRD0547X PRD0549X PRD1170X PRD1172X PRE0479X PRE0481X PRE1319X PRF0408X PRF0410X PRG0382X PRG1020X PRG1022X PRH0323X PRH0325X PRI0530X PRI0531X PRI1166X PRI1168X PRI1409X PRI1411X PRJ0480X PRJ0482X PRK0758X PRK0760X PRK1140X PRK1142X PRL0129X PRL0131X PRL0528X PRL0530X PSA0833X PSA0835X PSA1207X PSA1209X PSB0936X PSB0938X PSC0186X PSC0188X PSD0420X PSD0422X PSE0906X PSE0908X PSF0217X PSF0219X PSG0778X PSG0780X RQA1121X PRG0380X

Distribution pattern

Worldwide distribution--US Nationwide