PlainRecalls

Molded Products Inc

Compiled from official public sources by the publisher.

4 recalls on record · Latest: Apr 15, 2026

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Agency notice ledger

Federal filing book Molded Products Inc LIGHT-BOOK · SINGLE-AGENCY

#3,058 of 14,151 · 4 notices · 0.004% archive

  • BOOK 4 notices
  • RANK #3,058 of 14,151
  • SHARE 0.004% archive
  • AGENCY FDA Devices (4)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 15, 2026
  • PHOTO 1 Epic, LLC

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

Molded Products Inc 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 Molded Products Inc sits among 14,151 recalling firms

Molded Products Inc ranks 3,058th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Molded Products Inc vs all firms by recall-notice count

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

4 3058th 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 · 2026-09-14

Molded Products Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Molded Products Inc 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 Apr 15, 2026

See Luer Cap Set, MPC-130, set, administration, intravascular
FDA Devices Moderate Aug 28, 2019

Luer Lock Set - Catalog # MPC-125, for IV administration sets.
FDA Devices Moderate Apr 5, 2017

Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
FDA Devices Moderate Mar 27, 2013

Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing.

Molded Products Inc 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 Molded Products Inc? ▼
PlainRecalls indexes 4 distinct federal recall events naming Molded Products 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 Molded Products Inc sit among other recalling firms? ▼
Molded Products Inc ranks #3,058 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 Molded Products Inc's notices? ▼
FDA Devices accounts for 4 of this firm's 4 indexed notices.
What product category dominates Molded Products Inc's filing book? ▼
Filings for Molded Products 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.
Molded Products Inc: 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 Molded Products Inc; individual notices remain authoritative on each linked recall page.

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