PlainRecalls

Civco Medical Instruments Co. Inc.

Compiled from official public sources by the editorial team.

36 recalls on record · Latest: Apr 8, 2026

Civco Medical Instruments Co. Inc. Recall Insight

Civco Medical Instruments Co. Inc. appears on 36 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.035% 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 Apr 8, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 36 entries, severity tagging shows 0 critical, 36 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 36 of 36 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 (36). The date window on this page runs from Nov 25, 2015 to Apr 8, 2026.

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 Apr 8, 2026

eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149

FDA Devices Moderate Jun 11, 2025

BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers

FDA Devices Moderate Dec 29, 2021

VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX

FDA Devices Moderate Dec 29, 2021

VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX

FDA Devices Moderate Dec 29, 2021

VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX

FDA Devices Moderate Dec 29, 2021

VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX

FDA Devices Moderate Dec 19, 2018

SonoSite FUJIFILM Needle Guide Bracket, REF number P06013-08, Reusable non-sterile bracket for use with SonoSite L25 series transducers. Mfg for:

FDA Devices Moderate Dec 19, 2018

CIVCO Sales Demo Kit, REF DEMOGPGUIDE, for use by CIVCO and customer sales representatives.

FDA Devices Moderate Dec 19, 2018

CIVCO Biopsy Bracket, REF P03122-07, Reusable non-sterile single-angle bracket for use with SonoSite L25 series transducers.

FDA Devices Moderate Dec 19, 2018

SonoSite Needle Guide Bracket, REF numbers P06013-06 and P06013-07, Reusable non-sterile bracket for use with SonoSite L25 series transducers.

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Bracket, REF 674-057, Reusable non-sterile bracket for use with SonoSite L25 series tranducers, Rx.

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Starter Kit, REF 674-039, Reusable non-sterile bracket with sterile needle guides (1cm, 1.5cm, 2cm depths) with (10.2 x 147cm) CIV…

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Starter Kit, REF numbers P12922-01 and P12922-02, Reusable non-sterile bracket with sterile (1cm, 1.5cm, 2cm depths) needle guides…

FDA Devices Moderate Dec 19, 2018

SonoSite L25 Bracket Kit containing 1 Reusable non-sterile bracket, REF numbers P03122-01, P03122-02, P03122-03, P03122-04, and P03122-05, Mfg for:…

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Starter Kit, REF 674-037, Reusable non-sterile bracket with sterile needle guides (1.5cm, 2.5cm, 3.5cm, 4.5 depths) with (10.2 x 1…

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Starter Kit, REF 674-038, Reusable non-sterile bracket with sterile needle guide (1cm, 1.5cm, 2cm depths) with (10.2 x 147cm) CIV-…

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Bracket, REF P03122-06, Reusable non-sterile bracket for use with SonoSite L25/L25e transducers, Mfg by: CIVCO, Kalona, IA.

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Bracket, REF numbers M001457100, P06013-10, and P03122-08, reusable non-sterile single-angle bracket for use with SonoSite L25 ser…

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Starter Kit, REF numbers P12920-01 and P12920-02, Reusable non-sterile bracket with sterile (1.5cm, 2.5cm, 3.5cm, 4.5cm depths) n…

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Starter Kit, REF numbers P12924-01 and P12924-02, Reusable non-sterile bracket with sterile (1cm, 1.5cm, 2cm depths) needle guides…

FDA Devices Moderate Dec 19, 2018

CIVCO Needle Guide Bracket, REF 674-057-10, Reusable non-sterile bracket for use with FUJIFILM SonoSite, Inc. L25 series tranducers, Rx.

FDA Devices Moderate Sep 5, 2018

CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO

FDA Devices Moderate Sep 5, 2018

CIVCO Needle Guide, REF 676-144, QTY 24, STERILE EO

FDA Devices Moderate Aug 29, 2018

CIVCO lnfiniti Needle Guide Bracket. used for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers. …

FDA Devices Moderate Nov 25, 2015

CIVCO Biopsy Starter Kit, Reusable non-sterile bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. REFs 10787043, 11001906, 110019…

FDA Devices Moderate Nov 25, 2015

CIVCO Tracking Bracket Starter Kit, Reusable non-sterile PercuNav tracking bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. …

FDA Devices Moderate Nov 25, 2015

CIVCO Sales Demo Kit. REF DEMOGPGUIDE Large Gauge Infiniti Plus Needle Guides, used in needle-guided (or catheter) procedures with diagnostic ult…

FDA Devices Moderate Nov 25, 2015

CIVCO Needle Guide Starter Kit, Reusable non-sterile bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. REFs 674-030, 674-03…

FDA Devices Moderate Nov 25, 2015

CIVCO Infiniti Plus Needle Guide, Sterile Needle Guide, 12-18GA, Rx ONLY, STERILE EO. REFs 610-1215, 610-1234, 610-1235, 610-1236. Large Gauge …

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Civco Medical Instruments Co. Inc. with Zimmer Biomet, Inc. →

Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.