PlainRecalls

Blue Belt Technologies Mn

Compiled from official public sources by the publisher.

4 recalls on record · Latest: Jul 9, 2014

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Agency notice ledger

Federal filing book Blue Belt Technologies Mn LIGHT-BOOK · SINGLE-AGENCY

#2,806 of 14,151 · 4 notices · 0.004% archive

  • BOOK 4 notices
  • RANK #2,806 of 14,151
  • SHARE 0.004% archive
  • AGENCY FDA Devices (4)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 9, 2014
  • PHOTO 1 Epic, LLC

Nearest notice-volume peer: 1 Epic, LLC (0 notice gap)

Blue Belt Technologies Mn accounts for about 0.004% of the 104,423-notice archive on 4 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 →

Where Blue Belt Technologies Mn sits among 14,151 recalling firms

Blue Belt Technologies Mn ranks 2,806th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Blue Belt Technologies Mn vs all firms by recall-notice count

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

4 2806th of 14151 higher than 10,859 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 · 2026-09-15

Blue Belt Technologies Mn in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Blue Belt Technologies Mn holds about 0.004% of archive notices alongside 4 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 9, 2014

Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.
FDA Devices Moderate Jul 9, 2014

Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
FDA Devices Moderate May 21, 2014

NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.
FDA Devices Moderate Aug 28, 2013

Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.

Blue Belt Technologies Mn is a small archive contributor

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (4 here).

1 Epic, LLC 4 3rd Day Beverages LLC 4 A.p. Deauville, LLC 4 Aaa Pharmaceutical, Inc. 4 Aap Implantate Ag 4

Similar medical devices volume

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

Aap Implantate Ag 4 Ab Sciex, LLC 4 Accelerate Diagnostics Inc 4 Accord Media, LLC 4

Frequently Asked Questions

How many federal recall notices name Blue Belt Technologies Mn? ▼
PlainRecalls indexes 4 distinct federal recall events naming Blue Belt Technologies Mn, 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 Blue Belt Technologies Mn sit among other recalling firms? ▼
Blue Belt Technologies Mn ranks #2,806 of 14,151 by distinct recall-event count among 14,151 firms in this archive (77th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Blue Belt Technologies Mn's notices? ▼
FDA Devices accounts for 4 of this firm's 4 indexed notices.
What product category dominates Blue Belt Technologies Mn's filing book? ▼
Filings for Blue Belt Technologies Mn 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.
Blue Belt Technologies Mn: 4 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 Blue Belt Technologies Mn; individual notices remain authoritative on each linked recall page.

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