Windstone Medical Packaging, Inc.

Complete recall history across all FDA and CPSC categories, 315 total recalls

Windstone Medical Packaging, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (315)

FDA medical device enforcement actions by Windstone Medical Packaging, Inc.. Showing most recent 50.

Date Product Reason Class
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio Pac... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr F... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL KI... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Block Tra... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Heart Cat... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port Tray... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Loop... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 17, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Nerv... Windstone Medical Packaging issued a recall for specific item(s) and lot(s) o... Class II
Jun 8, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Lami... The recall notice was initiated due to a Medicom Urgent Medical Device Recall... Class II
Jun 8, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT ... The recall notice was initiated due to a Medicom Urgent Medical Device Recall... Class II
Jun 8, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Neur... The recall notice was initiated due to a Medicom Urgent Medical Device Recall... Class II
Jun 8, 2026 AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT ... The recall notice was initiated due to a Medicom Urgent Medical Device Recall... Class II
May 21, 2026 A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgica... Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal He... Class I
May 21, 2026 A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, surgi... Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal He... Class I
May 21, 2026 A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, ... Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal He... Class I
May 21, 2026 A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgi... Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal He... Class I
Apr 27, 2026 Aligned Medical AMS16835 Fluids Kit RX Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for ... Class II
Apr 2, 2026 Custom Convenience Kit containing recalled Medline Namic Angiographic Control... Affected kits contain Medline Namic RA Syringes, which are recalled by their ... Class I
Mar 11, 2026 Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14433 The product correction was initiated because B Braun is issuing a voluntary U... Class II
Mar 11, 2026 Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994A The product correction was initiated because B Braun is issuing a voluntary U... Class II
Mar 11, 2026 Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994 The product correction was initiated because B Braun is issuing a voluntary U... Class II
Aug 16, 2024 Aligned Medical Tonsil ENT Pack REF AMS9977 that contains the Cardinal Health... Due to convenience kits containing a kit component that is under a recall act... Class II
Aug 16, 2024 Aligned Medical Tonsil Pack REF AMS14809 that contains the Cardinal Health Sa... Due to convenience kits containing a kit component that is under a recall act... Class II
Aug 16, 2024 Aligned Medical Tonsil Tray REF AMS9300A that contains the Cardinal Health Sa... Due to convenience kits containing a kit component that is under a recall act... Class II
Aug 16, 2024 Aligned Medical T and A Pack REF AMS11482 that contains the Cardinal Health S... Due to convenience kits containing a kit component that is under a recall act... Class II
Aug 16, 2024 Aligned Medical Septo Pack REF AMS11480 that contains the Cardinal Health Sal... Due to convenience kits containing a kit component that is under a recall act... Class II
Dec 22, 2023 Aligned Medical Solutions, Local Lower Extremity Pack I, AMS10833, STERILEEO Sterility assurance for saline included in surgical kits cannot be guaranteed. Class I
Dec 22, 2023 Aligned Medical Solutions, Closure Kit, AMS13043, STERILEEO Sterility assurance for saline included in surgical kits cannot be guaranteed. Class I
Dec 22, 2023 Aligned Medical Solutions, In House Ocular Pack, AMS12947A STERILEEO Sterility assurance for saline included in surgical kits cannot be guaranteed. Class I
Dec 22, 2023 Aligned Medical Solutions, In House Ocular Pack, AMS12947, STERILEEO Sterility assurance for saline included in surgical kits cannot be guaranteed. Class I
Apr 24, 2023 Aligned Medical Solutions Spine Pack, REF: AMS4599(C, containing P 2 Cover ... Light handle covers may separate from the light handle (detach and fall off) ... Class II
Apr 24, 2023 Aligned Medical Solutions Minor Hand Pack, REF: AMS6539E, containing P 2 Co... Light handle covers may separate from the light handle (detach and fall off) ... Class II
Apr 24, 2023 Aligned Medical Solutions Hand Pack, REF: AmS4601E, containing P 2 Cover Li... Light handle covers may separate from the light handle (detach and fall off) ... Class II
Nov 1, 2022 Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product D... Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes th... Class II
Mar 21, 2022 Prevantics swabs and/or swabsticks contained inside the following Aligned Med... Convenience kits contain one or more swab/swabstick drug products, manufactur... Class II
Aug 19, 2021 Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 888157012... Monoject 0.9% Sodium Chloride Flush Syringe Manufactured by Cardinal Health a... Class I
Apr 8, 2021 Angio Pack REF: AMS8050A, Sterile EO, Contents:2 Glove Dermassist 7.5 PF PR ... Angio tubing included within Custom Convenience kits may contain insufficien... Class II
Apr 8, 2021 Angio Pack REF: AMS6908C, Sterile EO, Contents:1 Blade Scalpel # 11 SS 1 Bo... Angio tubing included within Custom Convenience kits may contain insufficien... Class II
Oct 24, 2017 AMS, ALIGNED MEDICAL SOLUTIONS, T&A Pack, AMS6357, STERILE EO. Custom surgical kits were manufactured with part #63310 Catheter Urethral 10F... Class II
Mar 16, 2017 Ortho Basic Pack, part number AMS6459 Product packaged in a convenient ma... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a conven... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Custom Tray, part numbers PSS1111 and PSS1111(A. Product packaged in a con... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Minor Operation Kit, part number AMS1530 Product packaged in a convenient ma... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Eye Cataract Pack, part numbers AMS1359 and AMS1359-1 Product packaged in a ... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a ... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Cataract Kit - Dr. Slingsby, part number CMP1017(B. Product packaged in a co... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 ENT Pack, part number AMS2727 Product packaged in a convenient manner for us... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner fo... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II
Mar 16, 2017 Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A Product packaged in... AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due... Class II

View all 315 device recalls →

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious, there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious, the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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