PlainRecalls

Windstone Medical Packaging, Inc.

Compiled from official public sources by the editorial team.

319 recalls on record · Latest: May 20, 2026

Windstone Medical Packaging, Inc. Recall Insight

Windstone Medical Packaging, Inc. appears on 319 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.314% 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 May 20, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 19 entries, severity tagging shows 0 critical, 19 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 19 of 19 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 (19). The date window on this page runs from Dec 16, 2015 to Oct 26, 2016.

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 Oct 26, 2016

Knee Scope Pack, Kit number AMS2498 and AMS2498(A convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Mohs Closer Pack, kit number PSS1827(A, PSS1827(B, and PSS1827(C convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Upper Torso Tray, Kit number PSS1554(B convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Nasal Pack, Kit number PSS2186 convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Surgical Pack, Kit number PSS3540 and PSS3540(A convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Vaginal Pack, Kit number AMS1722 convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Vein Kit - No Introducer TVS4027-NI(A convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Custom Venous Kit, TVS4024(C convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Bayview Abdominoplasty Pack, Kit part number 009079-1 convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Hystero Pack, Kit number PSS3535 convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

HSG Pack, Kit number PSS3287 convenience custom kits used for general surgery in hospital operating room

FDA Devices Moderate Oct 26, 2016

Custom Breast Augmentation Pack, Kit number PSS2455(B, PSS2455(C, PSS2455(D convenience custom kits used for general surgery in hospital operating r…

FDA Devices Moderate Oct 26, 2016

Dr Bragg Vein Tray - RX, kit numbers 007912-5, 007912-6, 007912-7, 007912-8 convenience custom kits used for general surgery in hospital operating r…

FDA Devices Moderate Oct 26, 2016

Breast Augmentation Pack, Kit part number AMS1786, AMS1786(A, AMS2790, AMS3324, AMS3324(A, and PSS3430. convenience custom kits used for general sur…

FDA Devices Moderate Jun 8, 2016

Laparotomy Pack Latex Free, part number 007725-7. This is a custom convenience surgical instrument disposable kit. There are multiple component…

FDA Devices Moderate Jun 8, 2016

General Surgery Pack, part number 006880-3. This is a custom convenience surgical instrument disposable kit. There are multiple component in th…

FDA Devices Moderate Jun 8, 2016

Laparotomy Pack, Part numbers 006268-8 and 007725-8. This is a custom convenience surgical instrument disposable kit. There are multiple compon…

FDA Devices Moderate Dec 16, 2015

AMS 4675 Angio Pack. For use in a general clinical procedure.

FDA Devices Moderate Dec 16, 2015

AMS 4674 Custom Pack. For use in a general clinical procedure.

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Windstone Medical Packaging, 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.