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

Major Kit, part number PHC1307(A

FDA Devices Moderate Mar 8, 2017

Total Hip Pack, part number PSS2956

FDA Devices Moderate Mar 8, 2017

Laparotomy Pack, part number 006268-9 Laparotomy Pack, part number AMS4418(A Laparotomy Pack, part number PSS2190(A

FDA Devices Moderate Mar 8, 2017

Laparoscopy Pack (1184), part number AMS6562

FDA Devices Moderate Mar 8, 2017

Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A

FDA Devices Moderate Mar 8, 2017

HSG Pack, part number PSS3287

FDA Devices Moderate Mar 8, 2017

Basic Setup Tray, part number AMS6414

FDA Devices Moderate Mar 8, 2017

Newport Coast Basic Pack, part number 007484-1

FDA Devices Moderate Mar 8, 2017

Arthroscopy Pack, part number AMS6559

FDA Devices Moderate Mar 8, 2017

General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General Pack, part number AMS5341 Gen…

FDA Devices Moderate Mar 8, 2017

C-Tray Pack, part number PSS2707(A

FDA Devices Moderate Mar 8, 2017

Basic Pack, part number AMS1868(B Basic Pack, part number AMS2608(A Basic Pack, part number AMS3861 Basic Pack, part number AMS4309 Basic Pack, p…

FDA Devices Moderate Mar 8, 2017

Major Laparotomy Pack - NS, part number AMS4347

FDA Devices Moderate Mar 8, 2017

Plastic Pack, part number PSS2462 Plastic Pack, part number PSS3319 Plastic Pack, part number PSS3319(A

FDA Devices Moderate Mar 8, 2017

Custom Venous Kit, part number TVS4024(C

FDA Devices Moderate Mar 8, 2017

D & C Kit, part number CMP1466(A

FDA Devices Moderate Mar 8, 2017

Eye Plastic Tray, part number PSS1931(A

FDA Devices Moderate Mar 8, 2017

Robotic Pack, part number AMS4389

FDA Devices Moderate Mar 8, 2017

Lap Band Pack, part number AMS1785(A

FDA Devices Moderate Mar 8, 2017

Custom Pack, part number AMS4776 Custom Pack, part number AMS4776(A Custom Pack, part number AMS5643 Custom Pack, part number AMS5643(A Custom Pa…

FDA Devices Moderate Mar 8, 2017

Bayview Breast Pack, part number 009080-2

FDA Devices Moderate Mar 8, 2017

Minor Pack, part number AMS3782(B Minor Pack, part number AMS3782(C Minor Pack, part number CMP1560 Minor Pack, part number PSS3518(B Minor Pack,…

FDA Devices Moderate Mar 8, 2017

Major Breast Pack, part number AMS3409(B

FDA Devices Moderate Mar 8, 2017

Lap Chole Pack (6037) , part number AMS6567

FDA Devices Moderate Mar 8, 2017

D&C/Cysto Pack, part number PSS3257(D

FDA Devices Moderate Mar 8, 2017

Hand Tray, part number PSS2365(F Hand Tray, part number PSS2365(G

FDA Devices Moderate Mar 8, 2017

Facial Tray, part number PSS1558(A

FDA Devices Moderate Mar 8, 2017

Knee Arthroscopy Pack , part number AMS2610(A Knee Arthroscopy Pack, part number AMS3236(A Knee Arthroscopy Pack, part numbre AMS3860

FDA Devices Moderate Mar 8, 2017

Foot Pack, part number AMS3637

FDA Devices Moderate Mar 8, 2017

Hip Pack (1347), part number AMS6564

FDA Devices Moderate Mar 8, 2017

Minor Procedure Pack, part number AMS4799

FDA Devices Moderate Mar 8, 2017

Breast Pack, part number AMS3238(A Breast Pack, part number AMS4419(A Breast Pack, part number AMS4419(B Breast Pack, part number AMS5750 Breast …

FDA Devices Moderate Mar 8, 2017

Laminectomy Pack, part number PSS1844(B

FDA Devices Moderate Mar 8, 2017

Morris Hysto Pack, part number PSS3198(A

FDA Devices Moderate Mar 8, 2017

Basic Face Kit, part number PS517A(D

FDA Devices Moderate Mar 8, 2017

Dr. Newman Surgical Procedure Pack, part number PSS1689(A

FDA Devices Moderate Mar 8, 2017

Anterior Cervical Fusion Pack, part number AMS2502(A Anterior Cervical Fusion Pack, part number AMS2502(C

FDA Devices Moderate Mar 8, 2017

Basic Kit, part number CMP1109(A

FDA Devices Moderate Mar 8, 2017

Minor Tray, part number AMS2685

FDA Devices Moderate Mar 8, 2017

Dr. Casey Pack, part number AMS4313(A

FDA Devices Moderate Mar 8, 2017

Lap Minor Pack (1346), part number AMS6566

FDA Devices Moderate Mar 8, 2017

Set-Up Pack, part number PSS1305(C

FDA Devices Moderate Mar 8, 2017

Laparoscopic Pack, part number AMS2499 Laparoscopic Pack, part number AMS2499(A Laparoscopic Pack, part number AMS2499(B

FDA Devices Moderate Mar 8, 2017

Open Procedure Pack II, part number RMS1740(A

FDA Devices Moderate Mar 8, 2017

Basic Tray, part number PSS1559(A

FDA Devices Moderate Mar 8, 2017

Head/Neck Pack, part number AMS6121

FDA Devices Moderate Mar 8, 2017

Shoulder Pack, part number AMS2936 Shoulder Pack, part number AMS3638 Shoulder Pack, part number AMS3711(B Shoulder Pack, part numbere AMS4212 Sh…

FDA Devices Moderate Mar 8, 2017

Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C

FDA Devices Moderate Mar 8, 2017

Extremity Pack, part number AMS3240 Extremity Pack, part number AMS4764 Extremity Pack, part number AMS4788(A Extremity Pack, part number PSS1798(…

FDA Devices Moderate Mar 8, 2017

Reduction Mammoplasty Pack, part number AMS4380 Reduction Mammoplasty Pack, part number AMS4380(B

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.