Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,301–7,350 of 15,271
- Class I
Food Recall · March 29, 2025
Bonya Strawberry-Banana Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .Undeclared Almonds
- Class I
Food Recall · March 29, 2025
Bonya Black Cherry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .Undeclared Almonds
- Class I
Food Recall · March 29, 2025
Bonya Mango Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .Undeclared Almonds
- Class I
Food Recall · March 29, 2025
Trader Joe's Hot Honey Mustard Dressing (SKU #80152), packaged in glass bottle with tamper overwrap on plastic cap, net wt. 12 fl. oz. UPC 0080 1522. DIST. & SOLD Exclusively by: Trader Joe's MonroviaUndeclared peanuts, soy, sesame, and wheat.
- Class I
Food Recall · March 29, 2025
Bonya Strawberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .Undeclared Almonds
- Class II
Medical Device Recall · March 28, 2025
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contPotential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
- Class II
Medical Device Recall · March 28, 2025
Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
- Class II
Medical Device Recall · March 28, 2025
Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
- Class I
Food Recall · March 28, 2025
Walker's Fruit Basket and Press House
Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallon bulk containersMay be contaminated with Clostridium botulinum
- Class II
Medical Device Recall · March 28, 2025
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contPotential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
- Unclassified
Consumer Product Recall · March 27, 2025
LaRose Industries LLC, dba Cra-Z-Art, of Randolph, New Jersey
Cra-Z-Art Gemex/Gel2Gem Jewelry KitsThe recalled jewelry-making kits contain a resin that, when liquid, can cause skin, eye and respiratory irritation or sensitization when inhaled, touched or ingested. The resin contains an acrylate (hydroxyethylmethacrylate "HEMA") in amounts prohibited in children's products by the Federal Hazardous Substances Act. Already created jewelry should be inspected to confirm it is fully cured. If there is liquid or any liquid residue present, the jewelry should not be worn and should be stored away from children. Once cured, the resin no longer presents the hazard.
- Unclassified
Consumer Product Recall · March 27, 2025
Specialized Bicycle Components Inc., of Morgan Hill, California
Specialized Vado and Como IGH E-Bikes with Chain GuardsThe bike's protective chain/belt guard does not cover the belt drive and loose clothing can get entrapped in the belt drive, posing a fall hazard.
- Class II
Medical Device Recall · March 27, 2025
Skytron Freedom 4FXS-60 Heavy Duty Monitor MountThe mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead to a failure of the mounting hardware and subsequent separation of the frame from the mounting column.
- Class II
Medical Device Recall · March 27, 2025
GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position catheters and other interventional devices within the Coronary and peripheral vaDue to a potential open seal in the sterile barrier packaging.
- Class II
Medical Device Recall · March 27, 2025
Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34, 00841268104792 KIT-002-35, 00841268104808 KIT-011-40, 00841268105553 KIT-011-62, 00841268105614 KIT-038-04, 008412681Due to a potential open seal in the sterile barrier packaging.
- Class II
Medical Device Recall · March 27, 2025
B Braun Interventional Coaxial Dilator REF: KIT-018-47, KIT-019-67, KIT-018-41, KIT-019-37 These Micro-Introducer Kits are intended to introduce up to a .038 inch guidewire or catheter into tDue to a potential open seal in the sterile barrier packaging .
- Class II
Medical Device Recall · March 27, 2025
Introducer Needle REF NDL-107-04 These needles are used for the percutaneous introduction of guidewiresDue to a potential open seal in the sterile barrier packaging.
- Class I
Food Recall · March 27, 2025
CFS CROMER FOOD SERVICES, INC. Anderson, SC 29621 CHICKEN SALAD On White NET WT. 4.3 OZ CONTAINS: EGGS, WHEAT, SOY UPC 31166 & UPC 13172Undeclared Milk - During an FDA inspection the firm was notified that milk was not declared on the label.
- Unclassified
Consumer Product Recall · March 27, 2025
Zhangzhou Jiesi Intelligent Technology Co. Ltd., of China
George Oliver DressersThe recalled dressers are unstable if they are not properly anchored to the wall, posing serious tip-over and entrapment hazards, and the two additional metal support legs also present tripping hazards. The dressers violate performance and warning label requirements of the STURDY Act.
- Class I
Medical Device Recall · March 27, 2025
Intraocular lens. enVista Monofocal IOL, All models starting with EE; enVista Aspire IOL, All models starting with EA; enVista Monofocal Toric IOL, All models starting with ETE; enVista Aspire ToriIn response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S.
- Class II
Medical Device Recall · March 27, 2025
GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in percutaneous fluid aspirations and small volume drainage procedures. For both adult and adolescent groups.Due to a potential open seal in the sterile barrier packaging .
- Class II
Food Recall · March 27, 2025
US Foods PREMIUM MONSTER COOKIE, 3 0Z Individually Poly film wrapped Ready to eat cookies, UPC 7 67367 10341 5. 52 Individually Poly film wrapped Ready to eat cookies per case, case UPC 107673671034Potential contamination with foreign material (plastic)
- Class II
Food Recall · March 27, 2025
5000642 CraftMark Oatmeal Cranberry Raisin Cookie Dough, 8 poly bags of 18 frozen pucks in a corrugate case, Net Weight 27.00 lbPotential contamination with foreign material (plastic)
- Class II
Food Recall · March 27, 2025
5000108 OATMEAL RAISIN COOKIE DOUGH, 6 poly bags of 30 frozen pucks in a corrugate case, Net Weight: 8.67 kg (19.12 lb)Potential contamination with foreign material (plastic)
- Class II
Medical Device Recall · March 27, 2025
Beckman Coulter DxI 9000 Access Immunoassay AnalyzerWhen DxI 9000 Access Immunoassay Analyzer is connected to a host system (laboratory information system (LIS) or middleware) and has accumulated canceled QC test results that were not sent by LIS, the analyzer may lose communication with the host system. The lost connection interrupts sample processing, which delays reporting patient test results and may subsequently delay patient treatment.
- Unclassified
Consumer Product Recall · March 27, 2025
Nutritional Fundamentals for Health (dba NFH), of Canada
NFH Iron SAP, NFH Heme Iron SAP and NFH Prenatal SAP bottlesThe recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.
- Unclassified
Consumer Product Recall · March 27, 2025
APOTHEKE, of Brooklyn, New York
APOTHEKE's Pumpkin Ginger 3-Wick Scented CandlesThe flame can burn too high and cause the candle to ignite and the glass container to break, posing fire, burn and laceration hazards.
- Class II
Medical Device Recall · March 27, 2025
B Braun Interventional ELITE HV Hemostasis Valve Introducer System REF 612802 Model Number: BCL-100-04 The Elite HV¿ Introducer System is indicated for use in percutaneous procedures to introducDue to a potential open seal in the sterile barrier packaging .
- Class I
Medical Device Recall · March 27, 2025
Intraocular Lens. enVista Envy IOL, All models starting with EN; enVista Envy Toric IOL, All models starting with ETN.In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S.
- Class II
Medical Device Recall · March 27, 2025
Introducer Kit- Tearaway MicroSlide REF KIT-051-01, 00841268106130 INT-101-15, 00841268107380 These introducers are used for the procedures to introduce catheters and other intravascular devicesDue to a potential open seal in the sterile barrier packaging.
- Unclassified
Consumer Product Recall · March 27, 2025
Delweld Industries Corp., of Stoystown, Pennsylvania
Children's Steel Utility Bunk BedsThe recalled children's bunk beds violate the federal regulations for bunk beds because the spacing between the guardrail and end support and the spacing around the mattress supports are greater than allowed, posing entrapment and strangulation hazards to children.
- Unclassified
Consumer Product Recall · March 27, 2025
Wenzhou Lingtuo Shangmao Youxiangongsi, dba LINKCOO, of China
LINKCOO Blackout Roller Window ShadesThe recalled window shades have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window shades are in violation of the federal regulations for window coverings and present a substantial product hazard. The window shades also violate federal regulations for labeling of window coverings.
- Class II
Drug Recall · March 26, 2025
Unisom, SleepMinis, Diphenhydramine HCl, Mini-Capsules, 25 mg, 60 Mini-Capsules bottles, Dist. by Chattem, Inc., P.O. Box 2219, Chattanooga, TN 37409-0219, USA, UPC 0 41167 00670 2CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities (NDSRI), N-nitroso-desmethyl-diphenhydramine (n-dph), above the FDA Recommended Intake Limit
- Class II
Food Recall · March 26, 2025
Desert Farms Jalapeno Mustard. Caution to refrigerate after opening. The shelf life is 2 years after the date of manufacture. It is packaged in 8 oz glass jars with a net wt. of 8.8 oz (249g). UPC codThe product is in violation for not having an approved filed process and for not having monitoring records.
- Class II
Medical Device Recall · March 26, 2025
The Trimble RTS873 robotic total station is a solution designed for construction professionals seeking precision, efficiency, and reliability in their layout tasks. The integrated Class 2 green aimingAn issue has been identified in the production of the RTS873 robotic total stations that may result in the green aiming laser output power being above its laser safety Class 2 classification.
- Class III
Food Recall · March 26, 2025
Cabot Creamery 8oz Extra Creamy Premium Butter, Sea Salted. Packaged as (2) 4oz sticks in cardboard shells; UPC: 0 78354 62038 0Product contaminated with elevated levels of coliform.
- Class II
Drug Recall · March 26, 2025
Breckenridge Pharmaceutical, Inc.
Duloxetine Delayed-Release Capsules, USP, 30 mg, Rx Only, 1,000 Capsules per bottle, Manufactured by: Towa Pharmaceutical Europe, S.L., Martorelles, (Barcelona), Spain, Distributed by: Breckenridge PhCGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the recommended interim limit.
- Class I
Food Recall · March 26, 2025
Tostitos Cantina Traditional Yellow Corn Tortilla Chips. Net Wt. 13oz. (368.5) UPC 0 28400-52848 1. Frito-Lay, Inc., Plano, TX 75024-4099.Undeclared allergen (milk).
- Class II
Food Recall · March 25, 2025
OLD WORLD SPICES & SEASONING, INC
Lillie's Q Buffalo Wing Sauce. Net wt. 13.5 oz, UPC 810069510972, Case label: Lillie's Q Buffalo Wing Sauce, Item # FGLOL422 Lot # 002125, 6/13.5 oz, UPC 10810069510979, BEST BY: JAN/21/2026Undeclared allergen (milk not listed as sub ingredient of butter). Milk also not listed in 'Contains' statement.
- Class II
Food Recall · March 25, 2025
Falafel King Enterprises, Inc.
Falafel King Taste the Mediterranean is a multi-component, 4 section plastic container, that includes Traditional Hummus, Falafel Balls, Tzatziki, and Mixed Vegetables. " Net Wt: 13 oz. UPC 8229862103Label declares tahini paste but does not declare sesame.
- Class II
Food Recall · March 25, 2025
Frosted Almond; 20 lbs (bulk); No UPC# Bulk Product Code: 23208elevated levels of aflatoxin
- Class II
Food Recall · March 25, 2025
Kashk (Whey) Ingredients: Whey, Water, Salt Nader Trading Inc., 1821 E. Dryer Road, Santa Ana, CA 92705 UPC# 685357001537Finished product label fails to include Milk in ingredient listing. (Undeclared Allergen)
- Class II
Food Recall · March 25, 2025
MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle (30 Serving). Manufactured exclusively for MTN OPS, LLC, 251 S Mountain Rd., Fruit Heights, UT. UPC 8 40359 40458 2Undeclared soy flour
- Class II
Medical Device Recall · March 25, 2025
restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number: HDL-060-C22L-000101 Acetabular Liner for Cordera Hip SystemThe hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.
- Class II
Medical Device Recall · March 24, 2025
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +3 Neck, Model Number 802602203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, UncementedThe associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stainless-steel femoral stems.
- Class II
Medical Device Recall · March 24, 2025
IceSeed 1.5 CX S NEEDLE OUS, Cryoablation Needle, REF H7493967334100. The needles are intended to convert high-pressure gas to either a very cold Freezing application or to a warm Thawing applicationBoston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings (see Affected Product Listing). Upon initial connection of an IceSeed CX needle to the Cryoablation System, the user will be prompted to perform the Needle Integrity and Functionality Test (NIT) per standard protocols. The affected needles perform as intended unless they are disconnected and reconnected to any channel after testing. In this case, the Cryoablation System will prompt re-execution of the NIT.
- Class II
Medical Device Recall · March 24, 2025
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, UncementedThe associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stainless-steel femoral stems.
- Class II
Medical Device Recall · March 24, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Intera 1.5T Power/Pulsar, Model Number: 781105;The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.
- Class II
Medical Device Recall · March 24, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
SmartPath to dStream for 1.5T, Model Number: 782146;The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.
- Class II
Medical Device Recall · March 24, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
SmartPath to dStream for 3.0T, Model Number: 782145;The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.