PlainRecalls

Reshape Medical Inc

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Nov 16, 2016

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Agency notice ledger

Federal filing book Reshape Medical Inc LIGHT-BOOK · SINGLE-AGENCY

#5,651 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,651 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 16, 2016
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Reshape Medical Inc accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Reshape Medical Inc's standing among 14,151 recalling firms

Reshape Medical Inc ranks 5,651st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Reshape Medical Inc vs all firms by recall-notice count

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

2 5651st of 14151 higher than 8,037 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 · 2026-09-14

Reshape Medical Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Reshape Medical Inc holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 16, 2016

ReShape Integrated Dual Balloon System, Gen 1, Model No. 01-0013-001, Catalog No. RSM110 product Usage: The ReShape Integrated Dual Balloon System is indicated for weight reduction when used in conjunction with diet and exercise, in obese patients with a Body Mass Index (BMI) of 30 40 kg/m2 and one or more obesityrelated comorbid conditions. It is indicated for use in adult patients who have failed weight reduction with diet and exercise alone.
FDA Devices Moderate Aug 24, 2016

ReShape Integrated Dual Balloon System, Gen 1, Catalog No. RSM110, Model No. 01-0013-001 The ReShape Integrated Dual Balloon System is indicated for weight reduction when used in conjunction with diet and exercise, in obese patients with a Body Mass Index (BMI) of 30 40 kg/m2 and one or more obesity related comorbid conditions. It is indicated for use in adult patients who have failed weight reduction with diet and exercise alone.

Reshape Medical Inc is a small archive contributor

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

Frequently Asked Questions

How many federal recall notices name Reshape Medical Inc? ▼
PlainRecalls indexes 2 distinct federal recall events naming Reshape Medical Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Reshape Medical Inc sit among other recalling firms? ▼
Reshape Medical Inc ranks #5,651 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Reshape Medical Inc's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Reshape Medical Inc's filing book? ▼
Filings for Reshape Medical 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.
Reshape Medical Inc: 2 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 Reshape Medical Inc; individual notices remain authoritative on each linked recall page.

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