Home / Brands / Windstone Medical Packaging
Windstone Medical Packaging Recalls
336 recalls on record · December 16, 2015 to August 5, 2026 · Medical Devices
Recalls by year
15
16
17
21
22
23
24
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 31, 2023Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Aligned Medical Solutions Hand Pack, REF: AmS4601E, containing P 2 Cover Light Handle Blue STE, Sterile EO
Hazard: Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient
May 31, 2023Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Aligned Medical Solutions Minor Hand Pack, REF: AMS6539E, containing P 2 Cover Light Handle Blue STE, Sterile EO
Hazard: Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient
May 31, 2023Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Aligned Medical Solutions Spine Pack, REF: AMS4599(C, containing P 2 Cover Light Handle Blue STE, Sterile EO
Hazard: Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient
January 11, 2023Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product Description 26000004M Custom Lasik Kit AMS
Hazard: Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes that have been recalled by 3M Healthcare.
May 25, 2022Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Prevantics swabs and/or swabsticks contained inside the following Aligned Medical Solutions convenience kits with Name/P
Hazard: Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International, that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products.
November 10, 2021Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 8881570121 inside the following Aligned Medical S
Hazard: Monoject 0.9% Sodium Chloride Flush Syringe Manufactured by Cardinal Health and placed into kits. Potential for the plunger to draw back after air has been expelled and reintroduce air back into the syringe.
June 23, 2021Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Angio Pack REF: AMS8050A, Sterile EO, Contents:2 Glove Dermassist 7.5 PF PR S 1 Bowl Fluid Containment W/LI 1 Cover P
Hazard: Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld
June 23, 2021Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Angio Pack REF: AMS6908C, Sterile EO, Contents:1 Blade Scalpel # 11 SS 1 Bowl Guidewire 80 oz 4 Clamp Towel 2.5 1 Co
Hazard: Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld
November 15, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls AMS, ALIGNED MEDICAL SOLUTIONS, T&A Pack, AMS6357, STERILE EO.
Hazard: Custom surgical kits were manufactured with part #63310 Catheter Urethral 10FR 16" which were subsequently recalled by CR Bard for a potential sterile barrier breach.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Vitrectomy Pack, part number AMS4952 Product packaged in a convenient manner for use in a general clinical procedure
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Vitrectomy Kit, part number CMP1016(A. Product packaged in a convenient manner for use in a general clinical procedure
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Setup Pack, part number AMS3112(A Product packaged in a convenient manner for use in a general clinical procedure
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls PRK Tray, part number DDS1044 Product packaged in a convenient manner for use in a general clinical procedure
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged in a convenient manner for use in a genera
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Ortho Basic Pack, part number AMS6459 Product packaged in a convenient manner for use in a general clinical procedur
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Ophthalmic Pack, Part number WAL1107(A and WAL1190 Product packaged in a convenient manner for use in a general clini
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Minor Operation Kit, part number AMS1530 Product packaged in a convenient manner for use in a general clinical procedur
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general clinical p
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Eye Cataract Pack, part numbers AMS1359 and AMS1359-1 Product packaged in a convenient manner for use in a general clin
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls ENT Pack, part number AMS2727 Product packaged in a convenient manner for use in a general clinical procedure
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A Product packaged in a convenient manner for use in a general c
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Dicken Eye Pack, part number CPA-3202-2. Product packaged in a convenient manner for use in a general clinical proced
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Custom Tray, part numbers PSS1111 and PSS1111(A. Product packaged in a convenient manner for use in a general clinica
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Cataract Pack, part numbers 008886-1, AMS2806, PSS3442, PSS3442(A, WAL1155, and WAL1155(A. Product packaged in a conven
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Cataract Kit - Dr. Slingsby, part number CMP1017(B. Product packaged in a convenient manner for use in a general clinic
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
April 19, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general clin
Hazard: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
March 8, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Vein Tray, part number AMS6312
Hazard: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.
March 8, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A
Hazard: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.
March 8, 2017Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Upper Torso Tray, part number PSS1554(B
Hazard: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.