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.
Read the official notice →- Date
- 2026-06-10
- Country
- United States
- Brand
- Windstone Medical Packaging
- Product
- Aligned Medical AMS16835 Fluids Kit RX
- Classification
- Class II
- Units
- US Nationwide distribution in the states of IL, VA.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2026-08-05
USWindstone 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 →- US
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…
FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of AZ, CA, CT, GA, IL, MA, MD, NY,…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 → - 2026-05-20
- 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 → - 2024-10-16
- US
Windstone Medical Packaging, Inc. recalls Aligned Medical Septo Pack REF AMS11480 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a…
Due to convenience kits containing a kit component that is under a recall action for improper use.
FDA · DeviceWindstone Medical Packaging, Inc.U.S. Nationwide distribution in the states of CA, MO, OH, VA, and WY.Official notice →
Other drugs & medical recalls in the United States
- 2026-06-10
- US
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product Description:…
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic…
FDA · DeviceIntuitive Surgical, Inc.U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA,…Official notice → - US
SSC- Surgical Specialties Corporation recalls Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
FDA · DeviceSSC- Surgical Specialties CorporationWorldwide - US Nationwide distribution in the states of Texas, Utah, Michigan…Official notice → - US
Grace Medical, Inc. recalls TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
Due to incorrect functional length on device labeling.
- US
GE Medical Systems China Co., Ltd. recalls MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical…
FDA · DeviceGE Medical Systems China Co., Ltd.Worldwide - US Nationwide distribution in the states of Florida and Georgia.…Official notice → - US
DeRoyal Industries Inc recalls DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
Sterile wound dressing, lacks sterility assurance
FDA · DeviceDeRoyal Industries IncUS Nationwide distribution in the states of FL & NC.Official notice → - US
CareFusion 303, Inc. recalls BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
FDA · DeviceCareFusion 303, Inc.US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ,…Official notice →