Safety Recalls

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15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 7,951–8,000 of 15,271

Medical Device Recall · February 13, 2025
Smiths Medical ASD, Inc.
smiths medical ProPort Plastic Venous Access System, Silicone Catheter, 2.87,,O.D. (8.4Fr) s 1.0mm I.D., REF 21-4150-24
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Class I
Drug Recall · February 13, 2025
Johnson, S C and Son, Inc
Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5%, zinc oxide 7.25%) packaged in a) 6 OZ (170 g) spray bottles UPC 813277019954 and UPC 813277019800; and b) Twinpack UPC 813277019930;
Chemical Contamination
Class II
Drug Recall · February 13, 2025
Zydus Pharmaceuticals (USA) Inc
Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1726-1; b) 6 x 50 mL Single-Dose Vial, NDC 70710-1726-8, Rx only, Manufactured by Zydus Lifesciences Ltd,
Failed Impurities/Degradation Specifications
Class II
Medical Device Recall · February 13, 2025
Smiths Medical ASD, Inc.
smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems, 82-24
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Class I
Medical Device Recall · February 13, 2025
Smiths Medical ASD, Inc.
smiths medical ProPort Low Profile Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm (5.8Fr) O.D. x 1.0mm., 6Fr Introducer, REF 21-4183-24
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Class I
Medical Device Recall · February 13, 2025
ZOLL Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S-10A, (7) G5S-11A, (8) G5S-80A-TSO, (9) G5S-80-L (1
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Class II
Medical Device Recall · February 13, 2025
Smiths Medical ASD, Inc.
Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127
Affected devices have a smaller diameter than expected and may potentially result in inadequate ventilation to the patient. Patient may experience hypoxia, underdose, or cardiopulmonary collapse.
Class I
Medical Device Recall · February 13, 2025
Smiths Medical ASD, Inc.
smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm O.D. (5.8 Fr) x 1.0mm I.D., REF 21-4152-24
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Class I
Medical Device Recall · February 13, 2025
MEDLINE INDUSTRIES, LP - Northfield
Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape.
Potential breach in pouch packaging which could lead to loss of sterility.
Class II
Medical Device Recall · February 13, 2025
ZOLL Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80C, (2) G5A-80C-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (A
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Class II
Consumer Product Recall · February 13, 2025
AFTCO Mfg. Co., of Santa Ana, California
Youth Solitude Jackets
The drawstring in the hood of the recalled jackets can get caught on objects and cause death or serious injury to children due to the strangulation hazard. The jackets are in violation of the federal regulations for children's upper outerwear and present a substantial product hazard.
Unclassified
Consumer Product Recall · February 13, 2025
Igloo Products Corp., of Katy, Texas
Igloo 90 Qt. Flip & Tow Rolling Coolers
The tow handle can pinch consumers' fingertips against the cooler, posing fingertip amputation and crushing hazards.
Unclassified
Consumer Product Recall · February 13, 2025
Setsmart LLC, of Brooklyn, New York
LoGest Climbing Ropes with Carabiners and LoGest Climbing Ropes with Heavy-Duty Metal Hooks
The climbing ropes can weaken and break, posing a fall hazard to consumers.
Unclassified
Consumer Product Recall · February 13, 2025
Umarex USA, of Fort Smith, Arkansas
T4E TR50 Air Pistols
The CO2 cartridge can be unintentionally ejected with force from the handle, posing an impact hazard.
Unclassified
Medical Device Recall · February 12, 2025
Becton Dickinson & Co.
BD BBL TB Stain Kit K, Catalog (REF): 212522
One component of the kit was shipped with an expiration date of 30Sep2024 while the Certificate of Analysis (COA) indicated an expiration date of 30Apr2025.
Class II
Medical Device Recall · February 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
namic convenience kits labeled as: KIT,ARTERIAL,60,(152CM),PG; medical convenience kit, REF 70036160
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Class II
Food Recall · February 12, 2025
Del Monte Foods, Inc
Good & Gather Cut Green Beans. Net Wt. 14.5 oz (411g). UPC 0 85239-11628 9. Dist. By Target Corporation, Minneapolis, MN 55403.
Foreign Object
Class II
Food Recall · February 12, 2025
The Fillo Factory Inc.
Chef's Line US Foods, 3 Grain Slider , 54/1.8 oz., Product in a plastic bag in a cardboard box. approx. 54 pieces per case. Keep Frozen,
Foreign material found in product (bolt)
Class II
Food Recall · February 12, 2025
Spicin Foods Inc
Noble Made Garlic Parmesan Wing Sauce, net wt 9.25oz, UPC 850000398542, #0897 BEST BY 06/02/2026 14:02 33724 L1, Code: F20920061
Customer complaints of bottles foaming when opened
Class II
Medical Device Recall · February 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
namic convenience kits labeled as: PML,72,ADULT,FLL-MLL,-,OEM, REF 80641722; medical convenience kit
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Class II
Medical Device Recall · February 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
namic convenience kits labeled as: MTS,COLOR,PML,KIT,-,FRENCH HOSPITAL PG; medical convenience kit, REF 600605710
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Class II
Medical Device Recall · February 12, 2025
MITO RED LIGHT INC
Mito Red Light, Super Mobile
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
Class II
Food Recall · February 12, 2025
The Fillo Factory Inc.
Chef's Line US Foods, 3 Grain Burger - 36/4.25 oz., Product in a plastic bag in a cardboard box. approx. 36 pieces per case. Keep Frozen,
Foreign material found in product (bolt)
Class II
Vehicle Recall · February 12, 2025
Hyundai Motor America
2023 GENESIS G90, 2024 GENESIS G90, 2025 GENESIS G90
Sudden, unintended braking increases the risk of a crash.
Unclassified
Medical Device Recall · February 12, 2025
MEDLINE INDUSTRIES, LP - Northfield
namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS,ST. *, REF 60010511; 3) MTS,LT,HT,KIT-BRYAN,LGH,M.C.,EAST, REF 60020323;
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Class II
Medical Device Recall · February 12, 2025
Zimmer, Inc.
Z1 Femoral Hip System, Product Number 611777612
There is a potential design issue with the Z1 Offset Stem Inserter leading to fracturing of the distal tip.
Class II
Drug Recall · February 12, 2025
Wuxi Medical lnstrument Factory Co., Ltd.
ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Carton, Sterile, Manufactured by Wuxi Medical Instrument Factory Co., Ltd., Made in C
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Class II
Food Recall · February 12, 2025
The Fillo Factory Inc.
Chef's Line US Foods, Black Bean Burger, 36/4.25 oz., Product in a plastic bag in a cardboard box. approx. 36 pieces per case. Keep Frozen,
Foreign material found in product (bolt)
Class II
Food Recall · February 12, 2025
JE Bakery 2019 LLC
Raisin Bran muffins, 6 count. Net Wt. 12.0 oz (0.75 lb) UPC 0 29341-00233 7. Labeled with the following store brands: Cub Foods, Jerrys Foods, and County Market
Undeclared allergen (walnuts)
Class I
Medical Device Recall · February 12, 2025
Remel, Inc
Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ system YV4000-VZ
Power supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.
Class II
Medical Device Recall · February 11, 2025
FUJIFILM Healthcare Americas Corporation
Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.
The incorrect computed patient age is showing in VX for patients less than 3 months old.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) GENERAL ENDOSCOPY PACK, Pack Number DYNJ44673G
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) ACL ARTHROSCOPY PACK, Pack Number DYNJ55316G; 2) ARTERIOGRAM PACK, Pack Number DYNJ64332; 3) ARTHRO PACK-LF, Pack Number DYNJ38748F; 4) ARTHRO PACK-LF, Pack
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) A & A KNEE PACK-LF, Pack Number DYNJHS0136D; 2) ABD CLOSURE PACK, Pack Number DYNJ56987B; 3) ADULT PERC PACK-LF, Pack Number PHS170994005A; 4) BASIC PACK, Pa
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) ANGIO PACK, Pack Number DYNJ50624A; 2) ANGIO PACK, Pack Number DYNJ30501F; 3) ANGIO PACK-LF, Pack Number DYNJ0954970G; 4) ANGIOGRAPHY 6 FRENCH PACK, Pack
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) EYE PACK, Pack Number VAL038BSCLC
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) AOP/BASIC EYE PACK-LF, Pack Number DYNJ0589795V; 2) CATARACT CM-LF, Pack Number DYNJ39921B; 3) CATARACT EYE, Pack Number DYNJ45662C; 4) CATARACT PACK, Pa
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) CT BIOPSY PACK, Pack Number DYNJ62734A; 2) E R C P PACK, Pack Number DYNJ44115A; 3) LARGE BIOPSY PACK NTX, Pack Number DYNJ68393A
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) ABLATION PACK, Pack Number DYNJ40629B; 2) ACH LAPAROSCOPIC GB PACK, Pack Number DYNJ67756A; 3) CHRISTUS WH LAP CHOLE PACK, Pack Number DYNJ60934B 4) CRMC
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) BILLINGS CLINIC SC HEAD & NECK, Pack Number DYNJ33656C; 2) BLEPH/RHINO PACK, Pack Number DYNJ64669A; 3) DB ENT CSTM PACK-LF, Pack Number DYNJ33585C; 4) DE
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ57622; 2) C SECTION PACK, Pack Number DYNJ48483B; 3) C SECTION PACK, Pack Number DYNJ61573; 4) C SECTION PACK, Pack Number DYN
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) L S GYN PACK, Pack Number DYNJ65616C; 2) MAIN CYSTO, Pack Number DYNJ61371A; 3) OB PACK-LF, Pack Number DYNJ20720C; 4) PELVISCOPY PACK-LF, Pack Number DY
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) CSMC/ABDOMINAL HYST PACK-LF, Pack Number DYNJ0665086F; 2) MAJOR VAGINAL HARPER PACK-LF, Pack Number DYNJ0161768D; 3) ROBOT LAP TOTAL HYST, Pack Number DYNJ
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) AV FISTULA PACK, Pack Number DYNJ80088; 2) AV FISTULA PACK-LF, Pack Number DYNJ0131782J; 3) CABG, Pack Number DYNJ906462B; 4) CABG ACCESSORY PACK-LF, Pac
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) CLOVIS ROBOTIC-LF, Pack Number DYNJ61061D; 2) CSMC/GYN LAPAROSCOPIC PACK-LF, Pack Number DYNJ0665103I; 3) DAVINCI PACK-RFD, Pack Number DYNJ47762O; 4) DA
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) ARTHROSCOPY PACK, Pack Number DYNJHS0101I; 2) ARTHROSCOPY PACK-LF, Pack Number DYNJ0390808F; 3) ARTHROSCOPY PACK-LF, Pack Number DYNJ23150J; 4) ARTHROSCO
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Food Recall · February 11, 2025
Trinidad Benham Corp
Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. Packaged in the U.S. UPC 0 70552 70412 1. DISTRIBUTED BY: WinCo Foods, LLC, BOISE, ID 83704
Elevated levels of MBC (carbendazim) thiophanate-methyl.
Class III
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II
Medical Device Recall · February 11, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline procedure kits labeled as: 1) LACERATION TRAY, Pack Number DYNJ17328B
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Class II