Safety Recalls
RSS ↗15,379 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 13,001–13,050 of 15,379
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926KA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) CYSTO, REF DYNJ905000D; b) ENDO KIT, REF DYKE1462A; c) ENDOSCOPY KIT, REF DYKE1431B; d) ENDOSCOPY KIT, REF DYKE1623B; e) GENERAL LAPAROA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYKE1410AA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ908566A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) GYN CDS, REF DYNJ905499B; b) GYN LAP, REF DYNJ909936; c) GYN LAPAROSCOPY, REF DYNJ902371J; d) GYN LAPAROSCOPY, REF DYNJ905509F; e) GYNA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. Part Number:Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) BASIC NASAL, REF DYNJ909932; b) BRONCH KIT, REF DYKE1007B; c) ENT, REF DYNJ909935; d) NASAL SINUS-LF, REF DYNJ902624G; e) ORAL, REF DA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289FA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) ARTHROSCOPY, REF DYNJ909699; b) BACK CDS, REF CDS984000C; c) EXTREMITY, REF DYNJ900847A; d) HAND-LF, REF DYNJ902619G; e) HIP PINNING CDA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
1,5L MED-SOFT LINER W/ 6MMX3M TUB. & ADULT VC, REF OR53929A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Drug Recall · March 22, 2024
Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00Lack of assurance of sterility: bags have the potential to leak..
- Class II
Medical Device Recall · March 22, 2024
20" Lead Wires, Replacement Part Number: 1067724-2Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) AAA CDS, REF CDS984011C; b) CAN KIT, REF DYKM1184; c) DENTAL CDS, REF CDS984010B; d) EGD KIT, REF DYK1253578F; e) EGD REG KIT, REF DYKA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYK1012268E1A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Drug Recall · March 22, 2024
IntegraDose Compounding Services LLC
fentaNYL Citrate 2,500 mcg/50mL in Sterile Water, 50 mL CADD for Injection, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-6030-1Lack of Assurance of Sterility: leaking bags
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PGA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones, Part NumbeDamage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
- Class II
Medical Device Recall · March 22, 2024
MEDLINE INDUSTRIES, LP - Northfield
1,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC, REF OR53926A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- Class II
Medical Device Recall · March 22, 2024
Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT Corporation) 120V Uninterruptable Power Supply Model: SCL500RM1U 2. APC (Schneider EPossible failure of Uninterruptable Power Supply (UPS) devices supporting the Patient Information Center (PIC) iX system, potential for the associated PIC iX system to shut down due to the lack of power. may lead to the delay in the detection of a change in a patient condition
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 125CM (5PK), REF H749085262302; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO RCB (5PK), REF H749085261902; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR1 (5PK), REF H74908526842; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class II
Food Recall · March 21, 2024
Tradewind Foods de Puerto Rico Inc.
Goya Red Kidney Beans, Net Wt.15.5oz.(439g), metal (tin) cans, 24 cans/15.5 oz. per caseDuring an FDA Inspection it was discovered swollen and leaking cans.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 155 (5PKX3), REF H749085263022; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.The failure to detect the partial obstruction in a 2.5mm sensor.
- Class I
Medical Device Recall · March 21, 2024
AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.The failure to detect the partial obstruction in a 2.5mm sensor.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL3.5 (5PK), REF H74908526212; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Unclassified
Consumer Product Recall · March 21, 2024
Nestlé USA Inc., of Arlington, Virginia
Metallic Mugs included in 2023 Holiday Starbucks-branded Gift SetsIf microwaved or filled with extremely hot liquid, the mugs can overheat or break, posing burn and laceration hazards.
- Class II
Food Recall · March 21, 2024
Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085L. mono contamination
- Class II
Food Recall · March 21, 2024
Great Value Twist & Shout Strawberry Creme Sandwich Cookies, Net WT 15.35 oz. box containing film wrapped trays of stacked cookies. 12 boxes per case.May contain foreign material (plastic)
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 (SGL), REF H74908526031; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL3 (5PK), REF H749085261002; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR2 (5PK), REF H74908526862; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (5PK), REF H74908526502; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265022; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed Monitor for airway monitoring.The failure to detect the partial obstruction in a 2.5mm sensor.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4 125CM (5PK), REF H749085262202; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG4 (5PK), REF H749085262532; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR3.5 (5PK), REF H74908526012; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG3.5 (5PK), REF H749085262522; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3 (5PK), REF H74908526573A2; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 125CM (5PK), REF H749085262352; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Drug Recall · March 21, 2024
Amneal Pharmaceuticals of New York, LLC
Vancomycin Hydrochloride for Oral Solution, USP, 250 mg per 5 mL, packaged as (a) 80 mL bottle, NDC 69238-2261-3; (b) 150 mL bottle, NDC 69238-2261-7; (c)300 mL bottle, NDC 69238-2261-5; Rx only, DisSuperpotent Drug: Due to overfilling of drug powder
- Unclassified
Consumer Product Recall · March 21, 2024
Crown Boiler Company LLC, of Philadelphia, Pennsylvania
Crown Aruba IV (AWR Series) gas-fired hot water boilersThe blocked vent switch (BVS) can fail to shut down the burners if the boilers are installed at altitudes above 2,000 feet and the vent system becomes blocked. In such an event, the boiler can emit excessive amounts of carbon monoxide into the building, posing a carbon monoxide (CO) poisoning hazard to consumers.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR6 (5PK), REF H74908526042; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 (5PK), REF H74908526022; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
- Class I
Medical Device Recall · March 21, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IM (5PK), REF H749085262012; cardiac catheterAn increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.