Abbott Vascular recalls Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus 30 Priority Pack w/.115 RHV - REF 1000185-115 WPL2122279-01…
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Read the official notice →- Date
- 2022-04-20
- Country
- United States
- Brand
- Abbott Vascular
- Product
- Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus 30 Priority Pack w/.115 RHV - REF 1000185-115 WPL2122279-01…
- Classification
- Class II
- Units
- U.S Nationwide Distribution.: AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Abbott Vascular recalls
- 2025-01-01
USAbbott Vascular Inc recalls 20/30 Priority Pack Accessory Kit w/Copilot, REF: 1003327, used for cardiovascular procedures.
Inflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or at the gauge, which could lead to air embolism.
FDA · DeviceAbbott Vascular IncUS: IA, MD, DC, IN, CA, NV, TX, CT, GA, MS, NY, OH, FL, NC, MI, KY, PA, VA,…Official notice →- 2022-10-26
- US
Abbott Vascular recalls Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT, MitraClip G4 Clip…
An increase in clip locking malfunctions, Establish Final Arm Angle and Clip Opening While Locked, have been observed. Contributing causes may be clip locking component material properties and certain use conditions.…
FDA · DeviceAbbott VascularWorldwide distribution - US Nationwide including in the states of PR, WA, NE,…Official notice → - 2022-05-25
- US
Abbott Vascular recalls Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO
There is a potential that the proximal marker may separate from the imaging catheter
FDA · DeviceAbbott VascularUS:AL AR AZ CA CO CT DC FL GA HI IA IL IN KS KY MA MD ME MI MN MO MT NC NE NH…Official notice →
Other drugs & medical recalls in the United States
- 2022-04-20
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
Product was improperly store which may cause a delay in results.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS distribution only - AL, CA, FL, GA, IL, IN, LA, MO, MS, NC, NE, NY, OH, PA,…Official notice → - US
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Fructosamine (Fruc), Siemens Material Number 11097637
Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent carryover impacting quality control (QC), patient samples, and calibrator results.
FDA · DeviceSiemens Healthcare Diagnostics, Inc.Global Distribution. US Nationwide.Official notice → - US
Philips North America, LLC recalls The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following product model #s:…
Update to instructions for use regarding the cleaning and disinfection process for the reusable probes.
FDA · DevicePhilips North America, LLCWorldwide distribution: US (nationwide) Including Puerto Rico and OUS…Official notice → - US
Luminex Corporation recalls Verigene Processor SP, Model Numbers: 10-0000-07 and 10-0000-07-R
Two of three complaints were initiated due to the customers repeatedly obtaining No Call results on the Processor SPs in question.
- US
GE Healthcare, LLC recalls MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c) 3101010-009, d) 3101010-008
Two scenarios may cause edits to measurements and diagnosis statements can be lost after a test is Signed in the MUSE NX web client.
FDA · DeviceGE Healthcare, LLCUS and Australia, Austria, Bahrain, Belgium, Brazil, Canada, Denmark, England,…Official notice → - US
Sensory Medical Inc recalls Cub 2 Enclosed Bed Canopy System
Due potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021.
FDA · DeviceSensory Medical IncU.S. Nationwide distribution to states including: AK, AZ, CA, CO, CT, DE, FL,…Official notice →