PlainRecalls

Carefusion

25 recalls on record · Latest: Sep 28, 2022

Carefusion Recall Insight

Carefusion appears on 25 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.025% 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 Sep 28, 2022, 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 Jul 7, 2021 to Sep 28, 2022.

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 Sep 28, 2022

BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock, REF: MX4436

FDA Devices Moderate Sep 28, 2022

BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433

FDA Devices Moderate Sep 28, 2022

BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171

FDA Devices Moderate Sep 28, 2022

BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141

FDA Devices Moderate Sep 28, 2022

BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS106

FDA Devices Moderate Sep 28, 2022

BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166

FDA Devices Moderate Sep 28, 2022

BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059

FDA Devices Moderate Sep 28, 2022

BD MaxGuard Extension Set with 4-way stopcock, REF: M4058

FDA Devices Moderate Sep 28, 2022

BD MaxGuard Extension Set, REF: ME1069

FDA Devices Moderate Sep 22, 2021

BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031; BD Gravity Burette Set 20 DROP 1.2 Micron Filte…

FDA Devices Moderate Sep 22, 2021

BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free Y-sites, REF: CM42500E-07; BD Gravity IV Set 3-port Closed Stopock Manifold B…

FDA Devices Moderate Sep 22, 2021

BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006

FDA Devices Moderate Sep 22, 2021

BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Tubing SmartSite Port (Burette) SmartSite Y-Site, REF: 10015012; BD Alaris Pump Infu…

FDA Devices Moderate Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

FDA Devices Moderate Sep 22, 2021

BD SmartSite Bag Access Device, REF: 2300E-0500; BD BAG ACCESS DEVICE CHECK VALVE SmartSite VALVE, REF: 2309E

FDA Devices Moderate Sep 22, 2021

BD SmartSite 'Y' Extension Set 2 Needle-Free Valves, REF: 20019E7D

FDA Devices Moderate Sep 22, 2021

BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED, REF: 42163E

FDA Devices Moderate Sep 22, 2021

BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD SmartSite J-LOOP Extension Set One Needle Free Valve, REF: 20021E7D; BD Sma…

FDA Devices Moderate Sep 22, 2021

BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing Disc, REF: 10798696; BD Syringe Set 20 DP MIC TBG CKV Anti-Siphon SmartSite …

FDA Devices Moderate Sep 22, 2021

BD Gravity Burette Set 60 DP 3 SmartSite VALVES BALL VALVE DRIP CHAMBER, REF: 10012564

FDA Devices Moderate Sep 22, 2021

BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve, REF: 2309E-0006

FDA Devices Moderate Sep 22, 2021

BD Alaris Pump Infusion Buerette Set Smallbore Tubing Smartsite Port (Burette) 3 SmartSite Y-Sites, REF: 2441-0006

FDA Devices Moderate Sep 22, 2021

BD Extension Set SMALLBORE Tubing SmartSite VALVE, REF: 10010511; BD SmartSite Extension Set Needle-Free Valve, REF: 10010912; BD EXTENSION SET SMAL…

FDA Devices Moderate Sep 22, 2021

BD ADD-ON Burette Set V/NV Needle-Free Valve, REF: 82113E-0006

FDA Devices Moderate Jul 7, 2021

MaxPlusTM bi fuse extension set with 2 clear needleless connectors - Product Usage: The needleless connector can be used for direct injection, inter…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Carefusion 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.