🏥 Medical Devices Class I - Dangerous
PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.
All Recalls
95,094 total recalls in our database
🏥 Medical Devices Class I - Dangerous
Product had torn/loose seal around the mouthpiece.
🏥 Medical Devices Class I - Dangerous
Potential for polystyrene particulate presence.
🏥 Medical Devices Class I - Dangerous
CareFusion has identified a potential risk associated with AVEA Ventilator caused by an incorrect F1 fuse on the AVEA Ventilator Transducer Communication Alarm (TCA) Board which may fail/blow, causing loss of power to the User Interface Module (UIM).
🏥 Medical Devices Class I - Dangerous
CareFusion has identified a potential risk associated with AVEA Ventilator caused by an incorrect F1 fuse on the AVEA Ventilator Transducer Communication Alarm (TCA) Board which may fail/blow, causing loss of power to the User Interface Module (UIM).
Excelsior Disposable Syringe Heparin Lock Flush, USP syringe (5 mL Fill in 10 mL syringe). For flushing of IV catheters and IV tubing only.
Excelsior Medical
🏥 Medical Devices Class I - Dangerous
Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml Syringe) failed Anti-Factor IIa assay for potency during testing of retention samples for heparin potency.
🏥 Medical Devices Class I - Dangerous
As a result of an internal investigation of a non-conformance it has been determined: 1) Depth Gauges from Lot UP15H2 exceed the overall length specification requirements. 2) Depth Gauges from prior lot numbers manufactured before Integra acquired the product line reflect an incorrect number for the first mm depth marking on the gauge. The number should be 4, it is 6. 3) The space / holder
Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 00587806538 POROUS PATELLA 41MM X 10MM - 00587806541
Zimmer Trabecular Metal Technology
🏥 Medical Devices Class I - Dangerous
Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
🏥 Medical Devices Class I - Dangerous
PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.
🏥 Medical Devices Class I - Dangerous
PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.
🏥 Medical Devices Class I - Dangerous
CareFusion has identified a potential risk associated with AVEA Ventilator caused by an incorrect F1 fuse on the AVEA Ventilator Transducer Communication Alarm (TCA) Board which may fail/blow, causing loss of power to the User Interface Module (UIM).
LCP Dia-Meta Volar Distal Radius Plate 15 H Shaft/LT-Sterile; Indicated for fractures, osteotomies, and non-unions of the radius and other small bones.
Synthes (USA) Products
🏥 Medical Devices Class I - Dangerous
Product incorrectly packaged. The labels on the outside of the box and on the LCP Dia-Meta Volar Distal Radius Plate inside the box are correct; however, the preprinted box which contains the LCP-Dia-Meta Volar Distal Radius Plate is incorrect. The box is preprinted for a 4.5 mm LCP Condylar Plate - Distal Femur.
Ecovent room sensors
Unknown Manufacturer
🏠 Consumer Products Class II - Moderate
The cover can come off during normal use, exposing high voltage components and posing an electrical shock hazard.
Octo-rattles
Unknown Manufacturer
🏠 Consumer Products Class II - Moderate
The fabric discs on the tentacles of the octopus rattles can detach, posing a choking hazard to young children.
Electric bottle and food warmers
Unknown Manufacturer
🏠 Consumer Products Class I - Dangerous
The warmers can overheat and catch on fire, posing a fire hazard to consumers.
Nuvi Global StemVitae Multivitamin 30oz.
Nuvi Global
🍎 Food Class I - Dangerous
Undeclared whey protein which contains the allergens of milk and soy lecithin.
7-Eleven Fresh To Go Sugar Cookie made with M&M (R) Chocolate Candy Net Wt 4.0 oz (114g). Manufactured by Bakery Express in Orlando, FL.
Bakery Express of Central Florida
🍎 Food Class I - Dangerous
Undeclared peanut allergen
🍎 Food Class I - Dangerous
Frozen Inc is recalling 24 oz RM German Chocolate Dessert Bar Cake because it does not list pecans.
🍎 Food Class I - Dangerous
Werner Brand Sweet Hot Crunch Mix is recalled because label declared butter, but milk is not declared.