Bard Peripheral Vascular Inc recalls REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr needle instead of a 6 Fr needle. They can be used in conjunction with the following drainage methods: Universal extension set and drainage bag,…
Read the official notice →- Date
- 2022-06-29
- Country
- United States
- Brand
- Bard Peripheral Vascular
- Product
- REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide distribution in the states of MS, NC,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Bard Peripheral Vascular recalls
- 2023-03-22
USBard Peripheral Vascular Inc recalls Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
The external diameter of the biopsy instrument is larger than the internal diameter of the coaxial needle, which could lead to: 1) Procedural delay, 2) Requirement of an additional device, 3), Needle tip breakage, if…
FDA · DeviceBard Peripheral Vascular IncWorldwide Distribution: US (Nationwide) includes states of: FL, MD, OH, CO,…Official notice →- 2023-02-15
- US
Bard Peripheral Vascular Inc recalls The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a nitinol stent…
An increase in the reported complaint rate for inability to deploy was identified and related to poor slide block bonding.
FDA · DeviceBard Peripheral Vascular IncWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice → - 2023-02-08
- US
Bard Peripheral Vascular Inc recalls Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter Repair Kit…
Due to the adhesive provided within the catheter repair kits maybe hardened/coagulated (unusable).
FDA · DeviceBard Peripheral Vascular IncWorldwide Distribution: U.S.(nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, DE,…Official notice → - 2022-03-23
- US
Bard Peripheral Vascular Inc recalls LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
FDA · DeviceBard Peripheral Vascular IncU.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA,…Official notice → - 2021-10-27
- US
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 → - 2021-10-13
- US
Bard Peripheral Vascular Inc recalls REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.
FDA · DeviceBard Peripheral Vascular IncWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →
Other drugs & medical recalls in the United States
- 2022-06-29
- US
Getinge Usa Sales Inc recalls Flow-c Anesthesia System : intended for use in administering anesthesia while controlling the entire ventilation of patient Product…
Potential for crack to form on the on/off switch of the suction unit, which may result in an unreasonable risk of harm to the patient. In the worst case, the switch can break, preventing the suction unit from being…
FDA · DeviceGetinge Usa Sales IncUS Distribution in states of Colorado, Florida, New Jersey, Indiana, Missouri,…Official notice → - US
Olympus Corporation of the Americas recalls EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus,…
Part (A-rubber) intended for a different model of gastrointestinal videoscope may have been used when replacing part on GIF-HQ190 during the last repair at Olympus. An Incorrect A-rubber fits tighter on the GIF-HQ190…
FDA · DeviceOlympus Corporation of the AmericasUS Nationwide distribution in the states of AL, FL, NC, NY.Official notice → - US
Olympus Corporation of the Americas recalls Colonovideoscope Model CF-H180AL
A (Camera unit) CCD intended for a different model of colonoscope may have been installed in the CF-H180AL, viewing angle would be narrower than a normal CF-H180AL and the use of EndoTherapy devices may stick out…
FDA · DeviceOlympus Corporation of the AmericasUS Nationwide distribution in the state of KY.Official notice → - US
Smiths Medical ASD Inc. recalls Medfusion Syringe Pump Models: 3500, 3500-0600-00, 3500-0600-01, 3500-0600-249, 3500-0600-50, 3500-0600-51, 3500-0600-82, 3500-306,…
Multiple issues with the potential for interruption of therapy or over-infusion: 1. Primary Audible Alarm (PAA), 2. Unanticipated Depleted Battery Alarms, 3. Time Base Alarm, 4. Intermittent Volume Over Time (IVOT) -…
FDA · DeviceSmiths Medical ASD Inc.Worldwide distribution. US nationwide including US Virgin Islands, Countries…Official notice → - US
Alcon Laboratories Ireland, Ltd recalls Alcon Clareon IOL with AutonoMe Delivery System
Due to device (preloaded intraocular lens) mislabeling, associated with partial mixing of product during overlapping manufacturing runs, and attributed to improper manufacturing line clearance.
FDA · DeviceAlcon Laboratories Ireland, LtdU.S.: AL, CA, FL, GA, IA, IL, KY, LA, MI, MO, NY, OH,OK, TX, VA, and WI…Official notice → - US
Medtronic Inc recalls HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
Batteries for the HVAD system have a weld defect affecting internal components within the HVAD battery, resulting in the battery to malfunction and no longer provide power or prevent the battery from holding a complete…
FDA · DeviceMedtronic IncWorldwide Distribution. US nationwide, Austria, Belgium, Finland, France,…Official notice →