PlainRecalls

Xeridiem Mediem Medical Devices Inc

Compiled from official public sources by the publisher.

105 recalls on record · Latest: Mar 2, 2016

Subscribe to new Xeridiem Mediem Medical Dev… recalls (RSS)

Agency notice ledger

Federal filing book Xeridiem Mediem Medical Dev… HEAVY-BOOK · SINGLE-AGENCY

#156 of 14,151 · 105 notices · 0.101% archive

  • BOOK 105 notices
  • RANK #156 of 14,151
  • SHARE 0.101% archive
  • AGENCY FDA Devices (105)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 2, 2016
  • PHOTO Lowlite Investments,…

Nearest notice-volume peer: Lowlite Investments, Inc. D/b/a Olympia Pharmacy (0 notice gap)

Xeridiem Mediem Medical Devices Inc accounts for about 0.101% of the 104,423-notice archive on 105 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Xeridiem Mediem Medical Dev…'s standing among 14,151 recalling firms

Xeridiem Mediem Medical Devices Inc ranks 156th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Xeridiem Mediem Medical Dev… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

105 156th of 14151 higher than 13,995 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-10-15

Xeridiem Mediem Medical Dev… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Xeridiem Mediem Medical Devices Inc holds about 0.101% of archive notices alongside 105 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026
FDA Devices Moderate Mar 2, 2016

EndoVive 3s Low Profile Balloon Kits Part Number: M00548850 (XMD P/N 70-0050-420) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The EndoVive 3s Low Profile Balloon is indicated for use in adult and pediatric patients who require long-term feeding, are unable to tolerate oral feeding, are at low risk for aspiration or require gastric decompression and/or
FDA Devices Moderate Mar 2, 2016

EndoVive 3s Low Profile Balloon Kits Part Number: M00549390 (XMD P/N 70-0050-922) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The EndoVive 3s Low Profile Balloon is indicated for use in adult and pediatric patients who require long-term feeding, are unable to tolerate oral feeding, are at low risk for aspiration or require gastric decompression and/or
FDA Devices Moderate Mar 2, 2016

EndoVive 3s Low Profile Balloon Kits Part Number: M00548560 (XMD P/N 70-0050-716) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The EndoVive 3s Low Profile Balloon is indicated for use in adult and pediatric patients who require long-term feeding, are unable to tolerate oral feeding, are at low risk for aspiration or require gastric decompression and/or
FDA Devices Moderate Mar 2, 2016

EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD P/N 70-0050-A18)
FDA Devices Moderate Mar 2, 2016

EndoVive 3s Low Profile Balloon Kits Part Number: M00548920 (XMD P/N 70-0050-B20) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The EndoVive 3s Low Profile Balloon is indicated for use in adult and pediatric patients who require long-term feeding, are unable to tolerate oral feeding, are at low risk for aspiration or require gastric decompression and/or

Xeridiem Mediem Medical Dev… carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Ameditech Inc 109 Medtronic Inc 109 Stryker Neurovascular 109 Jd & Sn Inc., dba Moses Lake Professional Pharmacy 101

Frequently Asked Questions

How many federal recall notices name Xeridiem Mediem Medical Dev…? ▼
PlainRecalls indexes 105 distinct federal recall events naming Xeridiem Mediem Medical Devices Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of October 2026). That count is an issuance inventory, not a hazard score.
Where does Xeridiem Mediem Medical Dev… sit among other recalling firms? ▼
Xeridiem Mediem Medical Devices Inc ranks #156 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Xeridiem Mediem Medical Dev…'s notices? ▼
FDA Devices accounts for 105 of this firm's 105 indexed notices.
What product category dominates Xeridiem Mediem Medical Dev…'s filing book? ▼
Filings for Xeridiem Mediem Medical Devices Inc span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Xeridiem Mediem Medical Devices Inc: 105 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Xeridiem Mediem Medical Devices Inc; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of October 2026