PlainRecalls

Churchill Medical Systems, Inc.

Compiled from official public sources by the editorial team.

16 recalls on record · Latest: Apr 29, 2015

Churchill Medical Systems, Inc. Recall Insight

Churchill Medical Systems, Inc. appears on 16 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.016% 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 29, 2015, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 16 entries, severity tagging shows 0 critical, 16 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 16 of 16 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 (16). The date window on this page runs from Mar 13, 2013 to Apr 29, 2015.

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 29, 2015

4" Trifurcated set with Bionectors and check valves, Product Code: BN-3082CV and BN-3083CV Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

4" Microbore T-Port Set, Product Code: BN-448 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

4" Microbore Trifurcated Ext set, Product Code: BN-308 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

6" Trifurcated set with Bionectors, Product Code: BN-944 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

4" Microbore Double Lumen Set with Bionector, Product Code: BN-208 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

6" Trifurcated Extension Set, Product Code: AMS-375-1 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

7" High Pressure Set with Bionector, Product Code: CMS-808 and CMS-808-1 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

8" Standard Bore Ext Set, Product Code: BN-481 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

Bifurcated set with check vales and Bionectors, Product Code: BN-2082CV Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 Accessory device used to administer medical fluids
FDA Devices Moderate Apr 29, 2015

Bifircated Extension Set, Product Code: BN-828 Accessory device used to administer medical fluids
FDA Devices Moderate Jan 29, 2014

AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.
FDA Devices Moderate Sep 25, 2013

Vygon 14 Microbore Extension Set with Bionector, CMS-814-1. The CMS-814-1 is a 14 inch extension set used to administer IV fluids.
FDA Devices Moderate Sep 25, 2013

Central Dressing Change Kit; AMS-8464CP- 6. Vygon Central Dressing Change Kit contains: 1 Pair Nitrile Gloves W/Wallet, Powderfree 1 Face Mask 1 Po…
FDA Devices Moderate Mar 13, 2013

Lifeguard Infusion Set with Smartsite, 20Ga, 1, CLGY-2010 Huber type needle set used for the infusion of medical fluids into implantable ports.

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Zimmer Biomet, Inc.

View recalls →

MEDLINE INDUSTRIES, LP - Northfield

View recalls →

Siemens Medical Solutions USA, Inc

View recalls →

FORD

View recalls →

Customed, Inc

View recalls →

Compare Churchill Medical Systems, 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.