PlainRecalls

Spectra Medical Devices, Llc

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Aug 19, 2026

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Agency notice ledger

Federal filing book Spectra Medical Devices, Llc LIGHT-BOOK · MULTI-AGENCY

#5,804 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,804 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Drug (1)
  • CAT medical devices
  • CATS 2 categories
  • LATEST Aug 19, 2026
  • PHOTO 3M Company

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

Spectra Medical Devices, Llc 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 →

Spectra Medical Devices, Llc's standing among 14,151 recalling firms

Spectra Medical Devices, Llc ranks 5,804th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Spectra Medical Devices, Llc vs all firms by recall-notice count

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

2 5804th 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 · 2026-10-09

Spectra Medical Devices, Llc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Spectra Medical Devices, Llc holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026

How the 2 notices break down

Same federal filing book as the hero total — split by issuing agency, no new counts.

FDA Devices Critical Aug 19, 2026

Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride Flush for IV tubing systems and indwelling intravascular access devices.
FDA Drug Moderate Jun 10, 2026

Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S. Korea, NDC 65282-1605-1.

Spectra Medical Devices, Llc is a small archive contributor

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

Similar medical devices volume

Nearest multi-notice firms that share this firm's dominant product category.

3M Company 2 3M Company/3m Espe Dental Products 2 A.o. Smith Electrical Products Co., of Tipp City, Ohio 2 Abbott Diagnostics Technologies As 2

Frequently Asked Questions

How many federal recall notices name Spectra Medical Devices, Llc? ▼
PlainRecalls indexes 2 distinct federal recall events naming Spectra Medical Devices, Llc, 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 Spectra Medical Devices, Llc sit among other recalling firms? ▼
Spectra Medical Devices, Llc ranks #5,804 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 Spectra Medical Devices, Llc's notices? ▼
FDA Drug accounts for 1 of this firm's 2 indexed notices across 2 issuing agencies.
What product category dominates Spectra Medical Devices, Llc's filing book? ▼
Filings for Spectra Medical Devices, Llc span 2 product categories, 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.
Spectra Medical Devices, Llc: 2 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Drug). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Spectra Medical Devices, Llc; individual notices remain authoritative on each linked recall page.

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