PlainRecalls

Stradis Healthcare, LLC.

30 recalls on record · Latest: Jul 15, 2015

Stradis Healthcare, LLC. Recall Insight

Stradis Healthcare, LLC. appears on 30 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.036% 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 15, 2015, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 30 entries, severity tagging shows 0 critical, 30 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 30 of 30 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 (30). The date window on this page runs from Jul 15, 2015 to Jul 15, 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 Jul 15, 2015

Lima Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Mississippi Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Arthroscopy Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Phleb Pack and Laser Phleb Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Shoulder Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Endovenous Kit, Endo Pack and Endovenous Laser Kit - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Vasc Custom Kit - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Skin and Vein Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Surgical Pack and General Surgery Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Head & Neck Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Blepharoplasty Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Suction Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

General Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Glaucoma Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Knee Arthro Pack and Knee Arthro Pack II - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Pediatric Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Custom Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Vaginal Rejuvenation Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Lipo Pack, Liposuction Expended Pack, and Liposuction Tray - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Standard Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Vein & Vascular Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Hand Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

ENT Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Plastic Pack and Plastic HNP Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Lipo/Buttocks Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Hand Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Face Lift Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Podiatry Pack - contains Devon Light Glove Used during surgery

FDA Devices Moderate Jul 15, 2015

Face Neck Pack - contains Devon Light Glove Used during surgery

Nearby Manufacturers

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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