PlainRecalls

WalkMed Infusion, LLC

Compiled from official public sources by the publisher.

19 recalls on record · Latest: Jul 27, 2016

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Agency notice ledger

Federal filing book WalkMed Infusion, LLC LIGHT-BOOK · SINGLE-AGENCY

#870 of 14,151 · 19 notices · 0.018% archive

  • BOOK 19 notices
  • RANK #870 of 14,151
  • SHARE 0.018% archive
  • AGENCY FDA Devices (19)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 27, 2016
  • PHOTO Abbott

Nearest notice-volume peer: Abbott (0 notice gap)

WalkMed Infusion, LLC accounts for about 0.018% of the 104,423-notice archive on 19 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

WalkMed Infusion, LLC's standing among 14,151 recalling firms

WalkMed Infusion, LLC ranks 870th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

WalkMed Infusion, LLC vs all firms by recall-notice count

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

19 870th of 14151 higher than 13,281 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

WalkMed Infusion, LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows WalkMed Infusion, LLC holds about 0.018% of archive notices alongside 19 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 27, 2016

T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
FDA Devices Moderate Jul 27, 2016

T100-022WF, IV Set with 2 Y-Sites, 0.22 micron filter, Back Check Valve, & FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T105-000WC IV Set w/2 Y-Sites, BC Vlv & Filter Cap. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
FDA Devices Moderate Jul 27, 2016

T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T100-000WF, IV Set with Upper Y-Site, Lower Y-Site, Back Check Valve, and Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Back Check Valve. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T100-000VF, IV Set with Lower Y Site and Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

Spike Set, 12" Microbore SPM-12. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T100-000F, 100" IV Set with Free Flow Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T090-022V 90" 20 Drop IV Admin Set Needle free Y-Site & 0.22 Fltr. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T095-022, IV Set with 0.22 Micron Filter. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Jul 27, 2016

T090-000V 90" 20 Drop IV Admin Set w/ Needlefree Y-Site. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
FDA Devices Moderate Nov 18, 2015

Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volumetric Infusion Pump). Used to pump fluids into a patient in a controlled manner.
FDA Devices Moderate Mar 12, 2014

Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for delivering infusions of medications, as well as providing TPN (Total Parenteral Nutrition) and PCA (Patient Control Analgesia). It is intended for use in hospitals, ambulatory & nursing home (extended care) settings, and home care environments.

WalkMed Infusion, LLC holds a measurable archive slice

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 (19 here).

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Adm Milling 19 Advance Pierre N 19

Similar medical devices volume

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

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Amo Puerto Rico Manufacturing, Inc. 19

Frequently Asked Questions

How many federal recall notices name WalkMed Infusion, LLC? ▼
PlainRecalls indexes 19 distinct federal recall events naming WalkMed Infusion, LLC, 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 WalkMed Infusion, LLC sit among other recalling firms? ▼
WalkMed Infusion, LLC ranks #870 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of WalkMed Infusion, LLC's notices? ▼
FDA Devices accounts for 19 of this firm's 19 indexed notices.
What product category dominates WalkMed Infusion, LLC's filing book? ▼
Filings for WalkMed Infusion, LLC 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.
WalkMed Infusion, LLC: 19 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 WalkMed Infusion, LLC; individual notices remain authoritative on each linked recall page.

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