Minivelle recall
Minivelle (estradiol transdermal system) Patches, Delivers 0.025 mg/day, 8 count boxes, Rx only, Mfd. by: Noven Pharmaceuticals, Inc. Miami, Florida…
Why was Minivelle recalled?
Defective Delivery System: out of specification results for shear, an attribute related to the adhesive properties of the transdermal patches.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lots: 82199 Exp. 12/2018; 83025 Exp. 05/2019
- Product
- Minivelle (estradiol transdermal system) Patches, Delivers 0.025 mg/day, 8 count boxes, Rx only, Mfd. by: Noven Pharmaceuticals, Inc. Miami, Florida…
- Recalling firm
- Noven Pharmaceuticals, Inc.
- Quantity
- 26217 boxes of 8 patches
- Distribution
- Nationwide
- Recall date
- October 3, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)