PlainRecalls

Instrumed International, Inc.

25 recalls on record · Latest: Dec 17, 2014

Instrumed International, Inc. Recall Insight

Instrumed International, Inc. appears on 25 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.030% 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 Dec 17, 2014, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 25 entries, severity tagging shows 0 critical, 25 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 25 of 25 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 (25). The date window on this page runs from Oct 8, 2014 to Dec 17, 2014.

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 Dec 17, 2014

D'errico perforator drills are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the Sym…

FDA Devices Moderate Dec 17, 2014

A zipser clamp is an instrument used to compress reduce blood flow to the penis and reduce pain and is sold under the Medline Industries, Boss Instru…

FDA Devices Moderate Dec 17, 2014

McKenzie enlarging burrs are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the CareF…

FDA Devices Moderate Dec 17, 2014

Gardner-Wells traction tongs are skull tongs for traction used to immobilize a patient with a cervical spine injury (e.g., fracture or dislocation) a…

FDA Devices Moderate Dec 17, 2014

Hudson cranial drill sets (w/ brace and 5 attachments) are bone cutting and drilling instruments that are used without a power source on a patient's …

FDA Devices Moderate Dec 17, 2014

A uterine tenaculum is a hook-like instrument used to seize and hold the cervix or fundus sold under the CareFusion, Teleflex Medical, Symmetry Surgi…

FDA Devices Moderate Dec 17, 2014

Schoitz weights are manual devices used with Schoitz tonometers and are intended to measure intraocular pressure by applying a known force on the glo…

FDA Devices Moderate Dec 17, 2014

A circumcision clamp is an instrument used to compress the foreskin of the penis during circumcision of a male infant sold under the Medline Industri…

FDA Devices Moderate Dec 17, 2014

An endometrial suction curette is a device used to remove material from the uterus and from the mucosal lining of the uterus by scraping and vacuum s…

FDA Devices Moderate Dec 17, 2014

McKenzie Perforator Drills are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the Pho…

FDA Devices Moderate Dec 17, 2014

Manual bunnell cranial drills are bone cutting and drilling instruments that are used without a power source on a patient's skull sold under the Boss…

FDA Devices Moderate Dec 17, 2014

Gardner-Wells wrenches are used in traction skull tongs for traction used to immobilize a patient with a cervical spine injury (e.g., fracture or dis…

FDA Devices Moderate Dec 17, 2014

Cloward Spanner gauges are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the CareFu…

FDA Devices Moderate Dec 17, 2014

Cushing perforating drills are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the Bos…

FDA Devices Moderate Dec 17, 2014

CVB distraction screws are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the Symmetr…

FDA Devices Moderate Dec 17, 2014

Titanium fixation screws, springloaded are used in traction skull tongs for traction used to immobilize a patient with a cervical spine injury (e.g.,…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

FDA Devices Moderate Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Instrumed International, Inc. with FORD →

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