Latest recalls — page 283
Older notices, newest first.
-
Highest risk · 1+ years ago
Blossom Children's Loungewear recall: Serious Risk of Injury or Death from Burns; Violates Mandatory Standard
Serious Risk of Injury or Death from Burns; Violates Mandatory Standard for Children's Sleepwear
-
Elevated risk · 1+ years ago
Doan's Bakery White Chocolate Coconut & Carrot Bundt Cakes recall: Undeclared allergens, wheat and milk
Undeclared allergens, wheat and milk
-
Class I · 1+ years ago
Scott & Jon's Shrimp Scampi with Linguini recall: Potential Listeria monocytogenes contamination
Potential Listeria monocytogenes contamination.
-
NHTSA safety recall · 1+ years ago
Toyota Tacoma and Tacoma Hybrid recall: The front driveshaft constant-velocity (CV) joint may deform and break
The front driveshaft constant-velocity (CV) joint may deform and break.
-
NHTSA safety recall · 1+ years ago
Toyota recall: A software error may cause the rearview image not to display when the vehicle
A software error may cause the rearview image not to display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the…
-
Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/10 recall: Systems may not perform as intended due to the deterioration of certain
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply…
-
Class II · 1+ years ago
Philips CT systems labeled as the following: 1. Brilliance iCT SP recall: The patient support table (couch) may descend unexpectedly to the lowermost
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
-
Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/20 recall: Systems may not perform as intended due to the deterioration of certain
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply…
-
Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 Product Codes: 722012 recall: Systems may not perform as intended due to the deterioration of certain
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply…
-
Class II · 1+ years ago
Philips CT systems labeled as the following: 1. Ingenuity Core128 / recall: The patient support table (couch) may descend unexpectedly to the lowermost
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
-
Class II · 1+ years ago
Ethicon, LLC Stratafix Spiral PDS Plus Bidirectional Knotless Tissue Control Device recall: Potential for barb non-engagement
Potential for barb non-engagement.
-
Class II · 1+ years ago
CooperVision, Inc. Sofmed Breathables, contact lens recall: One lot manufactured with an invalid sterilization cycle
One lot manufactured with an invalid sterilization cycle.
-
Class I · 1+ years ago
Medline medical convenience kits labeled as: 1. Newborn Resuscitation recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic…
-
Class II · 1+ years ago
Boston Scientific Corporation Extractor Pro RX Retrieval Balloon Catheter recall: The product in incorrectly labeled. The label indicates that the skive hole
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and…
-
Class II · 1+ years ago
Philips CT systems labeled as the following: 1. Ingenuity CT 728326 recall: The patient support table (couch) may descend unexpectedly to the lowermost
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
-
Class II · 1+ years ago
CooperVision, Inc. Voyant 1-Day Premium Toric, contact lens recall: One lot manufactured with an invalid sterilization cycle
One lot manufactured with an invalid sterilization cycle.
-
Class II · 1+ years ago
Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel recall: The patient support table (couch) may descend unexpectedly to the lowermost
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
-
Class II · 1+ years ago
Mindray North America BeneVision N1 Patient Monitor . Part Numbers: 6660E-PA00017 recall: Potential for activation of an abnormal alarm pause
Potential for activation of an abnormal alarm pause.
-
Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 Biplane OR Table Product recall: Systems may not perform as intended due to the deterioration of certain
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply…
-
Class II · 1+ years ago
Biofire Defense FilmArray Ngds Warrior Panel Ngds-Asy-0007 is a qualitative recall: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk
FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead…
-
Class II · 1+ years ago
Biomet, Inc. Juggerknot Mini Soft Anchors, Model/ recall: The outer carton box label is for the JuggerKnot 1.0mm Mini products
The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.
-
Class II · 1+ years ago
Philips CT systems labeled as the following: 1. Brilliance 16 Power recall: The patient support table (couch) may descend unexpectedly to the lowermost
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
-
Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/20 OR Table recall: Systems may not perform as intended due to the deterioration of certain
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply…
-
Class II · 1+ years ago
Philips CT systems labeled as the following: 1. CT 6000 recall: The patient support table (couch) may descend unexpectedly to the lowermost
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.