Access Vascular, Inc recalls HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package.
Read the official notice →- Date
- 2023-05-24
- Country
- United States
- Brand
- Access Vascular
- Product
- HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
- Classification
- Class II
- Units
- US distribution to States of: FL, TN, TX.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Access Vascular recalls
- 2023-10-25
USAccess Vascular, Inc recalls HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002
Specific lots of the Dual Lumen HydroPICC Kits were provided with the incorrect revision of the Instructions For Use (IFU) which do not include the following warnings statement: HydroPICC Dual Lumen Catheter is for…
FDA · DeviceAccess Vascular, IncUS Nationwide distribution in the states of IL, TX.Official notice →- 2023-03-01
- US
Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access system for…
Label with the incorrect component listed on the inner kit Tyvek header bag
FDA · DeviceAccess Vascular, IncUS Nationwide distribution in the states of CT, FL, NE, TN, TX, WA.Official notice → - US
Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous access system for…
Product Mislabeled on the outer bag and inner kit Tyvek header bag
FDA · DeviceAccess Vascular, IncUS Nationwide distribution in the states of FL, TX, WA.Official notice → - 2023-02-22
- US
Access Vascular, Inc recalls HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002
Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.
FDA · DeviceAccess Vascular, IncUS Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX.Official notice → - 2022-11-16
- US
Access Vascular, Inc. recalls Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserted Central Catheter
Scalpel and StatLock components packaged with specific lots of the HydroPICC catheter have a shorter expiration date than what is listed on the outer kit package.
FDA · DeviceAccess Vascular, Inc.Domestic distribution to NC, RI, NJ, and IL. No foreign distribution.Official notice →
Other drugs & medical recalls in the United States
- 2023-05-24
- US
TELEFLEX LLC recalls Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue tracts of femoral…
The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the product.
- US
3M Company - Health Care Business recalls 3M Attest Steam Chemical Integrators, REF 1243B
3M Attest Steam Chemical Integrators with dates of manufacture between November 6, 2022 and January 17, 2023 have an increased potential to leak ink during a sterilization cycle.
FDA · Device3M Company - Health Care BusinessWorldwide distribution: US (nationwide) and OUS (foreign) countries of:…Official notice → - US
Beckman Coulter Inc. recalls Beckman Coulter Bicarbonate, REF: OSR6137, 4x25 mL
There is a potential for a decrease in calibration ODs for Bicarbonate reagent which could result in calibration failures and/or quality control failures.
FDA · DeviceBeckman Coulter Inc.Worldwide Distribution: US (nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, DE,…Official notice → - US
Hiossen Inc. recalls ET III Nano-HA fixture System ET NH Dental Implant Model # ET3R5010B -Intended for Dental Implant Catalog #: AET3R5010B
Mis-labeled length of the dental implant on the Recall Implant's package. Dental implant size D5.0 x L8.5mm, labeled as D5.0 x L10mm
- US
- US
Surgical Innovations Ltd recalls YelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR
Optical Trocars sterility assurance can not be guaranteed