FDA Reports Ongoing Class II Recall of Medical Kits by Windstone Medical Packaging
An ongoing Class II recall involves 927 medical convenience kits distributed nationwide by Billings-based Windstone Medical Packaging, Inc.
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An ongoing Class II recall involves 927 medical convenience kits distributed nationwide by Billings-based Windstone Medical Packaging, Inc.
An ongoing FDA Class II recall covers 100 medical convenience kits containing recalled lidocaine.
Windstone Medical Packaging recalled 24 medical convenience kits containing Lidocaine due to supplier quality issues.
On August 5, 2026, the FDA classified the ongoing recall of 15 medical convenience kits packaged by Windstone Medical Packaging, Inc. as Class II.
The Food and Drug Administration considers the recall of 919 medical convenience kits carried out.
Windstone Medical Packaging recalled 3378 medical convenience kits containing Elevaris Lidocaine HCl injection due to supplier quality issues.
Windstone Medical Packaging recalled 950 convenience kits containing lidocaine injections recalled by their manufacturer over supplier quality issues.
The FDA has closed the recall action for 7,306 medical convenience kits distributed nationwide by Windstone Medical Packaging, Inc.
Windstone Medical Packaging is recalling 60 medical convenience kits across 22 states due to recalled lidocaine components.
An FDA enforcement report lists a seven-bottle recall of Vintage Roots Root Beer Syrup, distributed in Montana only, over an unapproved food additive.