Hydromorphone Hcl-bupivacaine Hcl-clonidine HCL PF recall: Sterility Concern
HYDROMORPHONE HCL-BUPIVACAINE HCL-CLONIDINE HCL PF INJECTABLE 21 mL syringes in two strengths: a) 20MG-20MG-60MCG/ML INJECTABLE, b) 5MG-5MG-100MCG/ML…
Why was Hydromorphone Hcl-bupivacaine Hcl-clonidine HCL PF recalled?
Non-Sterility
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?
Lot #: a) 09302020@30, BUD 10/23/2020, b) 10022020@14, BUD 10/30/2020
- Product
- HYDROMORPHONE HCL-BUPIVACAINE HCL-CLONIDINE HCL PF INJECTABLE 21 mL syringes in two strengths: a) 20MG-20MG-60MCG/ML INJECTABLE, b) 5MG-5MG-100MCG/ML…
- Recalling firm
- Med Shop Total Care Inc.
- Quantity
- 42 mL
- Distribution
- Texas and Puerto Rico
- Recall date
- August 18, 2021
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)