Smiths Medical ASD Inc. recalls medfusion Stopcock, 1-way and 4-way, Model Numbers (REF): a. 081-101BE b. 081-101GE c. 081-101GEE d. 081-101NE e. 081-102NE f. 081-102RE…
Product has a lack of sterility assurance
Read the official notice →- Date
- 2021-10-27
- Country
- United States
- Brand
- Smiths Medical ASD
- Product
- medfusion Stopcock, 1-way and 4-way, Model Numbers (REF): a. 081-101BE b. 081-101GE c. 081-101GEE d. 081-101NE e. 081-102NE f. 081-102RE…
- Classification
- Class II
- Units
- International Distribution to countries of: Armenia, Austria, Germany, Great…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Smiths Medical ASD recalls
- 2022-02-23
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Inadequate pouch seal leading to a compromised sterile barrier on products with a shaft length of 325mm.
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Two devices were labeled with the same serial number
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The labeling was missing information on sterilization and prohibition of reuse.
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Smiths Medical ASD Inc. recalls CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L…
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Other drugs & medical recalls in the United States
- 2021-10-27
- US
Kinsman Enterprises Inc recalls Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)
The belt may fail at lower loads than the labeled 600lbs.
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Limacorporate S.p.A recalls REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI: (01)08033390018852
There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included.
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Medtronic Xomed, Inc. recalls Medtronic Sterile single-use blades that are components of the StraightShot M Series Handpiece and Fusion ENT Navigation Software, and the…
There was an increase in complaints related to tip breaks and wobble/vibration.
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Bard Peripheral Vascular Inc recalls Catalog # BEK4511, Qty: 10, Ecomomy Jamshidi Bone Marrow Biopsy and Aspiration Tray, 11 G X 4"Biopsy/Aspiration needle, 15 G…
Due to misbranded products shipped to customers.
FDA · DeviceBard Peripheral Vascular IncU.S. Distribution: CA, GA,HI, IL, IN, LA, MO, MS, NC, OH, PA, PR, TX, UT, VA,…Official notice → - US
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The labeling was missing information on sterilization and prohibition of reuse.
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