Prevantics swabs and/or swabsticks contained inside the following Aligned Medical Solutions convenience kits with Name/P
Summary
The FDA issued a Class II for Prevantics swabs and/or swabsticks contained inside the following Aligned Medica by Windstone Medical Packaging, Inc.. Reason: Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International, that are subject to a drug .
Details
Source
Device Recall
External ID
Z-1101-2022
Action Date
2022-05-25
Status
Ongoing
Category
device
Product Description
Prevantics swabs and/or swabsticks contained inside the following Aligned Medical Solutions convenience kits with Name/Pack numbers: Ports Cath Pack (1794)/AMS6569, Minor Procedure Pack (20527)/AMS6570B, Breast Biopsy Pack (24771)/AMS6572A, Bone Marrow Pack (11862)/AMS6573, Ultrasound Biopsy Pack -Rx/AMS6828, Ultrasound Biopsy Pack -Rx/AMS6828A, C Access Tray/AMS9954, C Access Tray/AMS9954A, Access Tray A/AMS10234, Access Tray A/AMS10234A, C-Access Tray Chicago/AMS10236, C-Access Tray Chicago/AMS10236A, Access Tray/AMS10238, Access Tray/AMS10238A, Access Tray/AMS10238B, Gray Pack/AMS10247, Gray Pack/AMS10247A, C-Access Tray/AMS10249, C-Access Tray/AMS10249A, C Access Tray/AMS10255, C Access Tray/AMS10255A, Jacksonville Tray/AMS10256, Jacksonville Tray/AMS10256A, Jacksonville Tray/AMS10256B, NVS Access Tray/AMS10257, AZ Access Tray/AMS10271, AZ Access Tray/AMS10271A, Fistulagram/ C-Access Pack/AMS10280, Fistulagram/ C-Access Pack/AMS10280A, Ultrasound Tray w/PDI/AMS10710A, Procedure Tray/AMS10897A, Universal Block Tray-RX/AMS12381, Ultrasound Injection-RX/AMS12382, Pellet Insertion Tray/AMS12735, PICC Insertion Tray - RX/AMS-7192CS-8, Breast Biopsy Tray/DDS1010G, Single Shot Epidural Tray-Rx/DDS1149, PICC Insertion Tray-RX/VYMAXBASIC
Lot/Code Info: AMS6569/ Between 142683 and 170329; AMS6570B/ Between 150682 and 170330; AMS6572A/Between 150863 and 170779; AMS6573/Between 153041 and 167712; AMS6828/Between 154460 and 165574; AMS6828A/167575, 168392; AMS9954/Between 152386 and 157483; AMS9954A/Between 157481 and 169200; AMS10234/Between 152202 and 159363; AMS10234A/Between 158104 and 169113; AMS10236/Between 152782 and 156962; AMS10236A/Between 157478 and 169198; AMS10238/Between 150032 and 160155; AMS10238A/Between 159664 and 166692; AMS10238B/Between 167164 and 168646; AMS10247/Between 146572 and 156705; AMS10247A/Between 157182 and 168754; AMS10249/Between 158599 and 161959; AMS10249A/Between 157256 and 169105; AMS10255/Between 150385, and 156000; AMS10255A/Between 157201 and 167493; AMS10256/153691; AMS10256A/Between 158498 and 163451; AMS10256B/Between 160447 and 169108; AMS10257/Between 158004 and 166979; AMS10271/150057; AMS10271A/Between 157910 and 168755; AMS10280/Between 150046 and 158682; AMS10280A/Between 157914 and 168539; AMS10710A/Between 154520 and 164202; AMS10897A/162161, 163158, 163524; AMS12381/Between 154627 and 156334; AMS12382/153165; AMS12735/164426; AMS-7192CS-8/155088, 156610, 156611; DDS1010G/153351, 157709, 157746; DDS1149/167640; VYMAXBASIC/Between 156613 and 165673
Quantity Affected: 53,412
Reason for Recall
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.
Distribution
US: PA, WA, FL, GA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-21
Company
Billings, MT
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 164 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Windstone Medical Packaging, Inc. has 20 FDA actions in our database, including 20 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Windstone Medical Packaging, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Windstone Medical Packaging, Inc. have FDA actions?
Windstone Medical Packaging, Inc. has 20 FDA actions in our database, including 20 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1101-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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