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 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 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 (50). The date window on this page runs from Mar 8, 2017 to Mar 8, 2017.

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 Mar 8, 2017

Augmentation Pack, part number AMS6370

FDA Devices Moderate Mar 8, 2017

General Plastics Pack, part number 008617-1

FDA Devices Moderate Mar 8, 2017

Liposuction Pack, part number AMS3323(B Liposuction Pack, part number AMS5684 Liposuction Pack, part number AMS5699

FDA Devices Moderate Mar 8, 2017

Total Knee Pack (15710), part number AMS6563

FDA Devices Moderate Mar 8, 2017

GYN Pack, part number AMS4013(A

FDA Devices Moderate Mar 8, 2017

Lap Pack, part number AMS4801

FDA Devices Moderate Mar 8, 2017

Ocular Plastic Pack, part number AMS3868(A

FDA Devices Moderate Mar 8, 2017

Opgrande Hand Pack, part number AMS4767

FDA Devices Moderate Mar 8, 2017

Hysteroscopy Pack, part number AMS4797 Hysteroscopy Pack, part number AMS4797(A Hysteroscopy Pack, part number AMS4797(B

FDA Devices Moderate Mar 8, 2017

Extremity Pack (1344), part number AMS6561

FDA Devices Moderate Mar 8, 2017

Chest Breast Drape, part number AMS5853

FDA Devices Moderate Mar 8, 2017

Spine Pack , part number AMS3753(A Spine Pack, part number AMS3783(A Spine Pack, part number AMS3783(B Spine Pack, part number AMS6472

FDA Devices Moderate Mar 8, 2017

Shoulder Arthroscopy Pack, part number AMS2496(A Shoulder Arthroscopy Pack, part number AMS2496(B Shoulder Arthroscopy Pack, part number AMS2496(C …

FDA Devices Moderate Mar 8, 2017

Basic Setup Pack, part number AMS1787(A Basic Setup Pack, part number AMS6519

FDA Devices Moderate Mar 8, 2017

Basin Pack, part number AMS2497

FDA Devices Moderate Mar 8, 2017

Upper Extremity Pack, part number AMS4670 Upper Extremity Pack, part number AMS4670(A

FDA Devices Moderate Mar 8, 2017

Hystero Pack, part number PSS3535(A

FDA Devices Moderate Mar 8, 2017

Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D

FDA Devices Moderate Mar 8, 2017

Eye Tray, part number PSS1834 Eye Tray, part number PSS1834(A

FDA Devices Moderate Mar 8, 2017

Catheter Pack, part number AMS4399(A

FDA Devices Moderate Mar 8, 2017

Lipo Pack, part AMS4420(A

FDA Devices Moderate Mar 8, 2017

Ortho Minor Pack, part number AMS3710(A

FDA Devices Moderate Mar 8, 2017

Lap/Pelviscopy Pack, part number PSS3256(B

FDA Devices Moderate Mar 8, 2017

General Laparoscopy Pack, part number AMS4798 General Laparoscopy Pack, part number AMS4798(A

FDA Devices Moderate Mar 8, 2017

D & C Pack, part number AMS4796(A

FDA Devices Moderate Mar 8, 2017

General Plastic Pack, part number PSS2432(A

FDA Devices Moderate Mar 8, 2017

Bleph Pack, part number AMS3325(B

FDA Devices Moderate Mar 8, 2017

Basic Extended Pack, part number AMS4421(A Basic Extended Pack, part number AMS4421(B

FDA Devices Moderate Mar 8, 2017

Vein Tray, part number AMS6312

FDA Devices Moderate Mar 8, 2017

Custom Pack - with Introducer Kit, part number TVS4011NI(L

FDA Devices Moderate Mar 8, 2017

ENT Pack, part number AMS3237(A ENT Pack, part number AMS4214

FDA Devices Moderate Mar 8, 2017

Plastic Surgery Pack, part number AMS5685

FDA Devices Moderate Mar 8, 2017

Head Pack, part number PSS1934(B

FDA Devices Moderate Mar 8, 2017

Arthroscopy Pack, part number AMS2938 Arthroscopy Pack, part number AMS3639 Arthroscopy Pack, part number AMS4765 Arthroscopy Pack, part number PS…

FDA Devices Moderate Mar 8, 2017

Podiatry Pack, part number AMS2778 Podiatry Pack, part number AMS2778(A Podiatry Pack, part number AMS3785(B Podiatry Pack, part number AMS3785(C …

FDA Devices Moderate Mar 8, 2017

Total Joint Pack, part number 006358-6

FDA Devices Moderate Mar 8, 2017

Custom Breast Augmentation Pack, part number PSS2455(D

FDA Devices Moderate Mar 8, 2017

GYN Lap Pack, part number PSS2194(B

FDA Devices Moderate Mar 8, 2017

Hand Pack, part number AMS3640 Hand Pack, part number AMS4213(A Hand Pack, part number AMS4311(A Hand Pack, part number AMS5343 Hand Pack., part …

FDA Devices Moderate Mar 8, 2017

Peri GYN, part number PSS2193(A

FDA Devices Moderate Mar 8, 2017

Set Up Pack, part number PSS3574(A

FDA Devices Moderate Mar 8, 2017

Lumbar Laminectomy Pack, part number AMS2501 Lumbar Laminectomy Pack, part number AMS2501(A Lumbar Laminectomy Pack, part number AMS2501(B

FDA Devices Moderate Mar 8, 2017

Basic Pack (1185), part number AMS6560

FDA Devices Moderate Mar 8, 2017

Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.

FDA Devices Moderate Mar 8, 2017

Percutaneous Entry Kit, part number TVS4022(D Percutaneous Entry Kit , part number TVS4022(E Percutaneous Entry Kit, part number TVS4022(F

FDA Devices Moderate Mar 8, 2017

Open Procedure Pack, part number AMS4596 Open Procedure Pack, part number AMS4596(A Open Procedure Pack, part number AMS4596(B

FDA Devices Moderate Mar 8, 2017

Plastic Kit, part number CMP1084(C

FDA Devices Moderate Mar 8, 2017

Dr Bragg Vein Tray - RX, part number 007912-8

FDA Devices Moderate Mar 8, 2017

Dr. Landi EVLT Pack, part number AMS1483(E Dr. Landi EVLT Pack, part number AMS1483(E

FDA Devices Moderate Mar 8, 2017

Facial Pack , part number AMS6501

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.