PlainRecalls

Prytime Medical Devices, Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Feb 17, 2021

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Agency notice ledger

Federal filing book Prytime Medical Devices, In… LIGHT-BOOK · SINGLE-AGENCY

#5,594 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,594 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Feb 17, 2021
  • PHOTO 3M Company

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

Prytime Medical Devices, 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 →

Where Prytime Medical Devices, In… sits among 14,151 recalling firms

Prytime Medical Devices, Inc. ranks 5,594th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Prytime Medical Devices, In… vs all firms by recall-notice count

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

2 5594th 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 · 2026-09-28

Prytime Medical Devices, In… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Prytime Medical Devices, 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 Feb 17, 2021

PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA, SYRINGE, 30CC, STERILE 1 EA, INTRODUCER SHEATH KIT, 7 FR W/.035 SHORT GUIDEWIRE, STERILE 1 EA., PREFILLED, STERILE FIELD SALINE SYRINGE, 10 ML, 4 EA, CLAMP, 5 FR, STERILE, 1 EA, SCALPEL, #11SS, STERILE, 1 EA, SUTURE, NYLON, 18", 2-0, REVERSE CUTTING, STERILE 1 EA, THREE QUARTER DRAPE, STERILE 1 EA, INSERT, SALINE 1 EA, INSERT, CLAMP 1 EA UDI: (01) 0 0863092 00010 1
FDA Devices Moderate Dec 30, 2020

PryTime Medical - ER-Reboa Plus Catheter, Ref: ER7232PLUS, Guidewire Free, Compatabel with 7Fr introducer Sheaths, Arterial Line, Rx Only, UDI: (01) 0 0850001 10505 7 - Product Usage: intended for temporary occlusion of large vessels and blood pressure monitoring including patients requiring emergency control of hemorrhage.

Prytime Medical Devices, In… 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 Prytime Medical Devices, In…? ▼
PlainRecalls indexes 2 distinct federal recall events naming Prytime Medical Devices, 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 Prytime Medical Devices, In… sit among other recalling firms? ▼
Prytime Medical Devices, Inc. ranks #5,594 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 Prytime Medical Devices, In…'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Prytime Medical Devices, In…'s filing book? ▼
Filings for Prytime 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.
Prytime Medical Devices, 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 Prytime Medical Devices, Inc.; individual notices remain authoritative on each linked recall page.

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