Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number…
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 55998C due to potential for unexpected…
Read the official notice →- Date
- 2026-08-05
- Country
- United States
- Brand
- Windstone Medical Packaging
- Product
- AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number AMS15517;…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AZ, CA, CT, GA, IL, MA, MD, NY,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Windstone Medical Packaging recalls
- 2026-09-16
USWindstone Medical Packaging, Inc. recalls AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B
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 infusion port during manipulation.
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of CA, GA, WA.Official notice →- 2026-08-05
- US
Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Nerve Block Tray - RX, Part Number AMS13975A; 2)…
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to…
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IL, KS,…Official notice → - 2026-07-08
- US
Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit
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 dose audit.
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of PA, GA, CA, WA.Official notice → - 2026-06-10
- US
Windstone Medical Packaging, Inc. recalls Aligned Medical AMS16835 Fluids Kit RX
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of IL, VA.Official notice → - 2026-05-20
- US
Windstone Medical Packaging, Inc. recalls Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA…
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 connection or full disconnection…
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the state of Arizona.Official notice → - 2026-04-29
- US
Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994
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 utilized with BBMI s Infusomat Space…
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of GA, OR, TN, and WA.Official notice →
Other drugs & medical recalls in the United States
- 2026-08-05
- US
Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula,…
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ…
- US
Permobil Inc recalls M5 Corpus Power Wheelchair REF,120032
This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in…
FDA · DevicePermobil IncWorldwide - US: Nationwide distribution in the states of AL, AR, AZ, CA, CO,…Official notice → - US
Argon Medical Devices, Inc recalls L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may…
FDA · DeviceArgon Medical Devices, IncUS: AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC,…Official notice → - US
Permobil Inc recalls Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the…
FDA · DevicePermobil IncWorldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO,…Official notice → - US
Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within…
- US
Terex Utilities recalls Power Over Fiber Base Module
Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV", although Class 1 is appropriate for device. Improperly labeled - omitted…
FDA · DeviceTerex UtilitiesU.S. Nationwide Distribution and International DistributionOfficial notice →