Safety Recalls
RSS ↗15,379 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 13,851–13,900 of 15,379
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Drug Recall · January 30, 2024
Equate Lubricant Eye Ointment (Mineral Oil 42.5%, White Petrolatum 57.3%), Packaged in 3.5 gram tubes, Distributed by Walmart Inc., Bentonville, AR 72716, NDC 79903-026-35, UPC 681131395298Lack of Assurance of Sterility
- Class II
Food Recall · January 30, 2024
SPECIAL CAKE 53869 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
BLEACHED WHEAT FLOUR 5600352 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
2ND CLEAR 1051664 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Drug Recall · January 30, 2024
CVS Health Lubricant Eye Ointment (Mineral oil 31.9% Emollient, White petrolatum 57.7% Emollient), Packaged in in 3.5 gram tubes, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895Lack of Assurance of Sterility
- Class II
Food Recall · January 30, 2024
PIZZA 50/50 UNMALTED 904181 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
Applied Medical Resources Corp
Epix Universal Clip Applier, REF: CA500, STERILEEOTheir is the potential that Universal Clip applier may not load clip after the trigger is actuated.
- Class II
Food Recall · January 30, 2024
PIZZA FLOUR EN MA BL delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Drug Recall · January 30, 2024
Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%), Packaged in 3.5 g tubes, Distributed by Walmart Inc., Bentonville, AR 72716, NDC 79903-028-35, UPC 681131395304Lack of Assurance of Sterility
- Class II
Food Recall · January 30, 2024
01050 KA AP FLOUR delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
160919 FLR BLE WINTER delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-776Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Food Recall · January 30, 2024
43058751 BREAD FLR delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
The recalled Reser's Amish Macaroni Salad was packaged in a plastic clear container where the top lid is labeled as Reser's Amish Macaroni Salad, Net Wt. 1lb., and the container side label indicates RUndeclared Wheat. The recalled Reser's Amish Macaroni Salad was packaged in a plastic container where the top lid is correctly labeled as Reser s Amish Macaroni Salad but the container side label mis-labeled as Reser s Southern Style with Egg Potato Salad. The ingredient statement on the Reser s Southern Style with Egg Potato Salad container side label does not declare wheat.
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Food Recall · January 30, 2024
BREAD FLOUR UNBL ENR delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-758Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Food Recall · January 30, 2024
15953 ALL PURPOSE EN EZ BL delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
2-00007-0000 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-762Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 30, 2024
Applied Medical Resources Corp
Epix Universal Clip Applier, REF: CA500, STERILEEO included within the following kit Reference Numbers: GK1003, AME Kit 54562 GK1004, KIT LAP CHOL DEN HOED 2, GK1005, K2550 - H¿PATECTOMIE ERASME,Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.
- Class II
Food Recall · January 30, 2024
PB AP delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Food Recall · January 30, 2024
DRIED SOFT 75 ENR 134348 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-774Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Drug Recall · January 30, 2024
Lubricant PM Ointment (Mineral Oil 42.5% and White Petrolatum 57.3%), Packaged in 3.5 gram tubes, Distributed by: AACE Pharmaceuticals, Inc., Fairfield, NJ 07004, NDC 71406-124-35, UPC 371406124356Lack of Assurance of Sterility
- Class II
Food Recall · January 30, 2024
PIZZA 50/50 UNMALTED delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
9200458510 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
2-04585-0000 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
1002560 DONUT CAKE FLR delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
2-15969-0000 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
HARD WHEAT 2ND CLEAR delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 4F X 10 CM STD .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-749Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Food Recall · January 30, 2024
UNBLE ENR MALTED RM6144 FLOUR delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Food Recall · January 30, 2024
HARD E6 1036 delivered as bulk product in approximately 50,000 lbs trailersPotential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-752Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-765Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. - Catalog Number: 45-781Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Class II
Medical Device Recall · January 29, 2024
Waldemar Link GmbH & Co. KG (Mfg Site)
Embrace Drill Tower, Standard/Lateral (25mm)The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of the instruments.
- Class II
Medical Device Recall · January 29, 2024
Olympus Corporation of the Americas
SOLTIVE Premium SuperPulsed Laser (TFL-PLS )A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.
- Class II
Medical Device Recall · January 29, 2024
NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and replacement of a flow-compromised filter during treatment of acute and chronic reProduct is recalled due to reports of blood leaking or spraying from the arterial line on the cartridge.If this failure occurs, a patient may experience uncontrolled blood loss or a healthcare professional could be exposed to infectious patient blood.
- Class II
Medical Device Recall · January 29, 2024
Canon Medical System, USA, INC.
MRI system: Vantage Orian, Vantage Fortian, Model: MRT-1550For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.
- Class II
Medical Device Recall · January 29, 2024
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
Shimadzu, Trinias, Digital Angiography SystemDue to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
- Class II
Medical Device Recall · January 29, 2024
Canon Medical System, USA, INC.
Vantage Titan, Model: MRT-1504For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.
- Class II
Medical Device Recall · January 29, 2024
Waldemar Link GmbH & Co. KG (Mfg Site)
Embrace Drill Tower, Wedged (25mm)The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of the instruments.