PlainRecalls

Terumo Medical Corporation

15 recalls on record · Latest: Jul 31, 2019

Terumo Medical Corporation Recall Insight

Terumo Medical Corporation appears on 15 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.018% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Jul 31, 2019, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 15 entries, severity tagging shows 2 critical, 13 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 15 of 15 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (15). The date window on this page runs from Jul 3, 2013 to Jul 31, 2019.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280

FDA Devices Moderate Jul 31, 2019

Terumo Needle, 23G x 1", Product Code NN2325R

FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 20G x 1", Product Code 100204

FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 1", Product Code 100211

FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215

FDA Devices Moderate Jul 31, 2019

Terumo Needle, 18G x 1", Product Code NN1825R

FDA Devices Moderate Jul 31, 2019

Terumo Needle, 30G x 1/2", Product Code NN3013R

FDA Devices Critical Jun 5, 2019

SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425, STFI-1435, STFI-1625, STFI-1635, STFI-1825, STFI-1835, STFI-192…

FDA Devices Critical Jun 5, 2019

Portico Solo Re-Collapsible Access System , Model Numbers PRTSOLO-19, PRTSOLO-20

FDA Devices Moderate Mar 7, 2018

Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath is designed to be used for t…

FDA Devices Moderate May 10, 2017

Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.

FDA Devices Moderate May 10, 2017

SurFlo IV Catheter

FDA Devices Moderate Sep 14, 2016

PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Intro…

FDA Devices Moderate Jul 3, 2013

Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction …

FDA Devices Moderate Jul 3, 2013

Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through the skin into a vein or arter…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds