Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,251–3,300 of 15,186
- Class II
Medical Device Recall · November 14, 2025
Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.Potential for incomplete seal on header bag.
- Class I
Medical Device Recall · November 14, 2025
GE Medical Systems China Co., Ltd.
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012-9620-000; Carestation 620 A1, REF 1012-9620-200;Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure. Anesthesia systems only operate on battery power in a rare event that AC mains power is lost and there is no continuous backup emergency power. If AC power is interrupted, the system will not automatically switch over to the battery supply mode and will reboot. If this issue occurs, a temporary disruption of mechanical ventilation, manual ventilation, and volatile agent delivery may occur. Following the reboot, the system will not return to the previous ventilation settings.
- Class II
Medical Device Recall · November 14, 2025
Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.Potential for incomplete seal on header bag.
- Class II
Food Recall · November 14, 2025
CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Distributed by: Venzu Traders LLC venzutraders@outlook.comPotential contamination with heavy metal (lead).
- Class II
Drug Recall · November 14, 2025
Cinacalcet Hydrochloride Tablets, 90 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-412-02CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Class II
Medical Device Recall · November 14, 2025
Halyard, EP LAB PK. Catalog Number: ESJH009-03.Potential for incomplete seal on header bag.
- Class I
Medical Device Recall · November 14, 2025
GE Medical Systems China Co., Ltd.
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012-9750-002; Carestation 750c A1, REF 1012-9755-000Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure. Anesthesia systems only operate on battery power in a rare event that AC mains power is lost and there is no continuous backup emergency power. If AC power is interrupted, the system will not automatically switch over to the battery supply mode and will reboot. If this issue occurs, a temporary disruption of mechanical ventilation, manual ventilation, and volatile agent delivery may occur. Following the reboot, the system will not return to the previous ventilation settings.
- Class I
Food Recall · November 13, 2025
Dry Roasted Baking Macadamia Nuts, Unsalted Halves Ideal for Baking, Cooking, Salads or Ice Cream; NET WT 20 OZ (1 LB 4 OZ) 567g UPC: 8 60011 44301 8Potential Salmonella contamination.
- Unclassified
Consumer Product Recall · November 13, 2025
Shantou Chenghai Xingzigu Toy Industry Co., Ltd., of China
Bettina Doll Set with Magic Light UnicornThe doll sets violate the mandatory standard for toys because the battery compartment of the unicorn contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · November 13, 2025
Great Lakes Wholesale International of Lockport, Illinois
Great Lakes Select Button Cell and Coin BatteriesThe button cell and lithium coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. If a child swallows button cell or coin batteries, the ingested batteries can cause serious injuries, including internal chemical burns and death.
- Class II
Food Recall · November 13, 2025
Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug with red plastic lid, UPC 041250841197, Dist. By Meijer Distribution, Inc. Grand Rapids, MI 49544, packed 4 per caseFloating black foreign substance in the product
- Class II
Medical Device Recall · November 13, 2025
InPen App, Model/CFN Number: MMT-8061 (Android Users)When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't choose to allow notifications to override phone settings when on mute/Do Not Disturb, and previously set up override permission is deleted, so audible and vibratory notifications not received, which may lead to delayed insulin therapy, hyperglycemia.
- Class II
Drug Recall · November 13, 2025
Ganirelix Acetate Injection, 250 mcg/0.5mL, Single-dose Sterile Prefilled Syringe, 27 gauge by 1/2' needle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, United States, ManFailed impurities/degradation specifications: out of specification results for Ganirelix acetate acrylic acid adduct impurity.
- Class II
Medical Device Recall · November 13, 2025
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
- Class II
Medical Device Recall · November 13, 2025
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
- Class III
Food Recall · November 13, 2025
Olive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edible salt, white sugar, monosodium glutamate, licorice, cloves, food additives (citric acid, DL malicProducts contain banned sweetener: cyclamates.
- Class III
Food Recall · November 13, 2025
DADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash, edible salt, soybean oil, edible vinegar, white granulated sugar, spices, food additives (sodium glProducts contain banned sweetener: cyclamates.
- Class II
Food Recall · November 13, 2025
Jeni's Splendid Ice Creams LLC
Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton with Item UPC: 850060644122, packed 8 retail cartons per case with Case UPC: 1085006Undeclared allergens - wheat and soy
- Class II
Medical Device Recall · November 13, 2025
Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the recall is potential performance issues found in the Alinity ci-series System software versions 3.6.1. and lower that could lead to erroneous results for multiple analytes. The issue was identified by Abbott during the internal testing of complaint investigations.
- Class II
Medical Device Recall · November 13, 2025
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818KSome products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
- Unclassified
Consumer Product Recall · November 13, 2025
Belkin International Inc., of El Segundo, California
Portable Power Banks and Wireless Charging StandsThe lithium-ion battery in the power banks and charging stands can overheat, posing fire and burn hazards to consumers.
- Unclassified
Consumer Product Recall · November 13, 2025
Trek Bicycle Corporation, of Waterloo, Wisconsin
Trek and Electra-branded Bicycles with Coaster Brakes and Replacement Rear Wheels with Coaster BrakesThe coaster brakes can fail to engage, resulting in the rider losing control, posing a crash hazard.
- Unclassified
Consumer Product Recall · November 13, 2025
Certain Tesla Powerwall 2 AC Battery Power SystemThe lithium-ion battery cells in certain Powerwall 2 systems can cause the unit to stop functioning during normal use, which can result in overheating and, in some cases, smoke or flame and can cause death or serious injury due to fire and burn hazards.
- Unclassified
Consumer Product Recall · November 13, 2025
Zippee Activity ToysThe recalled silicone activity toys contain spherical ends that can reach the back of the throat, posing a serious choking hazard to children.
- Unclassified
Consumer Product Recall · November 13, 2025
Changzhoulongzhiyuedianzishangwuyouxiangongsi dba Zigjoy-US, of China
Zigjoy Toddler Sleep Sacks with FeetThe recalled sleep sacks violate the mandatory flammability standard for children's sleepwear, posing a burn hazard and risk of serious injury or death to children.
- Unclassified
Vehicle Recall · November 12, 2025
2024 GMC CANYON, 2025 GMC CANYON, 2026 GMC CANYONAn air bag that deploys improperly increases the risk of injury in a crash.
- Class II
Medical Device Recall · November 12, 2025
1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450Products may contain contamination, which may result in a darker or brown media color.
- Class II
Medical Device Recall · November 12, 2025
The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emitting diodes (LEDs) as well as an electronics control unit foWhen the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.
- Class II
Food Recall · November 12, 2025
Brass Langri Cookware Sticker label: 14Potential contamination due to leachable lead.
- Unclassified
Vehicle Recall · November 12, 2025
2025 BMW X3, 2026 BMW X3Unintended steering wheel movement while the vehicle is stationary increases the risk of an injury and on the road, a crash.
- Class II
Drug Recall · November 12, 2025
Medical Products Laboratories, Inc.
Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
- Class I
Food Recall · November 12, 2025
Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable mylar bag, UPC 850053365126, Manufactured For: Genepro Protein, Inc. 15000 Weston PaProduct is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
- Class I
Food Recall · November 12, 2025
Stuffed Foods brand Cacio e Pepe Arancini; KEEP FROZEN; For institutional use only; Ready-to-cook; Cook to internal temp. of 165oF; Case pack: 3/3 lbs; Net Weight: 9lbs; UPC 00819985020787Undeclared Soy Protein Concentrate
- Class II
Medical Device Recall · November 12, 2025
ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-sterile; CT5502T ChemoPlus Full Coverage Gown, Closed Back, Regular/Medium, MedAffected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
DEXLOCK Achilles Repair Implant Kits, MAKT4520There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical procedure.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class I
Medical Device Recall · November 11, 2025
Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08Devices are not suitable for organ transplant.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.
- Class II
Medical Device Recall · November 11, 2025
Olympus Corporation of the Americas
Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in urological applications.Complaints of the ceramic tip of the resection sheath breaking have been received.