Fresh Recalls

Windstone Medical Packaging recalls

22 recent recalls on record for Windstone Medical Packaging in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

A M S (4)AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as (12)AMS Convenience Kit (1)Aligned Medical AMS16835 Fluids Kit RX (1)Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes wit (1)Custom Convenience Kits Pre Op Kit - NS (3)

All Windstone Medical Packaging recalls

FDA Class II · Medical device · September 16, 2026

AMS Convenience Kit recall — Windstone Medical Packaging, Inc.

The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the i…

Official ID Z-3138-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2819-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2818-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2817-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2816-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2815-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2814-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2813-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lid…

Official ID Z-2812-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Official ID Z-2802-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Official ID Z-2801-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Official ID Z-2800-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Official ID Z-2799-2026 · Official record ↗

FDA Class I · Medical device · July 8, 2026

A M S recall — Windstone Medical Packaging, Inc.

Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …

Official ID Z-2622-2026 · Official record ↗

FDA Class I · Medical device · July 8, 2026

A M S recall — Windstone Medical Packaging, Inc.

Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …

Official ID Z-2621-2026 · Official record ↗

FDA Class I · Medical device · July 8, 2026

A M S recall — Windstone Medical Packaging, Inc.

Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …

Official ID Z-2620-2026 · Official record ↗

FDA Class I · Medical device · July 8, 2026

A M S recall — Windstone Medical Packaging, Inc.

Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …

Official ID Z-2619-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Aligned Medical AMS16835 Fluids Kit RX recall — Windstone Medical Packaging, Inc.

Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.

Official ID Z-2307-2026 · Official record ↗

FDA Class I · Medical device · May 20, 2026

Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes wit recall — Windstone Medical Packaging, Inc.

Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose …

Official ID Z-2066-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Custom Convenience Kits Pre Op Kit - NS recall — Windstone Medical Packaging, Inc.

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …

Official ID Z-1921-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Custom Convenience Kits Pre Op Kit - NS recall — Windstone Medical Packaging, Inc.

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …

Official ID Z-1920-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Custom Convenience Kits Pre Op Kit - NS recall — Windstone Medical Packaging, Inc.

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …

Official ID Z-1919-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.