Home / Brand archive
43 reported ongoing
47 records in this archive. Latest source date Jul 26, 2024.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
Reports have been received regarding open seals on the packaging.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of CA, FL, GA, IL, MA, ME, MI, NC, NY, PA, and WV. There was government distribution.
Teleflex received reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: -failure of the intra-aortic balloon to completely inflate over its full l...
Class IReported ongoing
Distribution: Worldwide distribution. US nationwide including Puerto Rico, AU, BA, BE, BG, BN, CA, CL, CN, CO, CY, CZ, DE, EC, ES, FR, GB, GP, GR, HU, HK, IE, IL, IN, IQ, IT, JO, JP, KW, KZ, ...
Teleflex received reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: -failure of the intra-aortic balloon to completely inflate over its full l...
Class IReported ongoing
Distribution: Worldwide distribution. US nationwide including Puerto Rico, AU, BA, BE, BG, BN, CA, CL, CN, CO, CY, CZ, DE, EC, ES, FR, GB, GP, GR, HU, HK, IE, IL, IN, IQ, IT, JO, JP, KW, KZ, ...
Teleflex received reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: -failure of the intra-aortic balloon to completely inflate over its full l...
Class IReported ongoing
Distribution: Worldwide distribution. US nationwide including Puerto Rico, AU, BA, BE, BG, BN, CA, CL, CN, CO, CY, CZ, DE, EC, ES, FR, GB, GP, GR, HU, HK, IE, IL, IN, IQ, IT, JO, JP, KW, KZ, ...
Teleflex is initiating this voluntary recall for the above-mentioned products due to reports received indicating a potentially defective component. The complaints received relate to resistance of the guidewire handle/chamber during use. The possible immedia...
Class IReported ongoing
Distribution: Worldwide distribution: US (nationwide) and OUS (foreign) to countries of: AE, AR, AT, AU, BE, BH, BR, CA, CN, CO, CY, DE, EC, EE, ES, FR, GR, HK, HR, IT, KW, LB, LU, MX, MY, NL...
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Class IReported ongoing
Distribution: US
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Class IReported ongoing
Distribution: US
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Class IReported ongoing
Distribution: US
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Class IReported ongoing
Distribution: US
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Class IIReported ongoing
Distribution: US Nationwide distribution.
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Class IIReported ongoing
Distribution: US Nationwide distribution.
Potential for catheter separation or leakage
Class IReported ongoing
Distribution: Nationwide distribution. International distribution to Canada.
There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.
Class IReported terminated
Distribution: US Distributor in states of: FL, GA, KY, OH, PA and WV.
There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.
Class IReported terminated
Distribution: US Distributor in states of: FL, GA, KY, OH, PA and WV.
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
Class IReported ongoing
Distribution: Worldwide
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 47 records, including 43 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.