WalkMed Infusion, LLC

Complete recall history across all FDA and CPSC categories — 19 total recalls

WalkMed Infusion, LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (19)

FDA medical device enforcement actions by WalkMed Infusion, LLC

Date Product Reason Class
Jun 14, 2016 T090-000V 90" 20 Drop IV Admin Set w/ Needlefree Y-Site. Packaged in a Tyvek ... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T095-022, IV Set with 0.22 Micron Filter. Packaged in a Tyvek pouch, with 50 ... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T090-022V 90" 20 Drop IV Admin Set Needle free Y-Site & 0.22 Fltr. Packaged i... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T100-000F, 100" IV Set with Free Flow Clip. Packaged in a Tyvek pouch, with 5... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 Spike Set, 12" Microbore SPM-12. Packaged in a Tyvek pouch, with 50 pouches p... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch, with... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T100-000VF, IV Set with Lower Y Site and Free Flow Clip. Packaged in a Tyvek ... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Back Check Valve. P... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch, with... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch, wit... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T100-000WF, IV Set with Upper Y-Site, Lower Y-Site, Back Check Valve, and Fre... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch, with 50 pouches... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 The pump (with cushioning foam inserts) is packaged in a single pump box. Fou... WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton Infusi... Class II
Jun 14, 2016 T105-000WC IV Set w/2 Y-Sites, BC Vlv & Filter Cap. Packaged in a Tyvek pouch... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 T100-022WF, IV Set with 2 Y-Sites, 0.22 micron filter, Back Check Valve, & FP... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Jun 14, 2016 The pump (with cushioning foam inserts) is packaged in a single pump box. Fou... WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton Infusi... Class II
Jun 14, 2016 T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch, with 50 po... WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton A... Class II
Oct 1, 2015 Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000... The device might fail to detect air in line while infusing the medication Ven... Class II
Feb 17, 2014 Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton... WalkMed Infusion is initiaing a recall on their Triton FP Infusion Pump, Part... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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