Safety Recalls
RSS ↗15,362 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 8,101–8,150 of 15,362
- Class II
Medical Device Recall · February 10, 2025
Candida ID Antigen, REAG, AG, REF C50110, Vol 1 mL REF ID1001, Immy Fungal Antigens, Positive Controls, & Immunodiffusion (ID) plates for use in the ID test, RX only, IVD, CECandida Immunodiffusion Antigen may have reduced sensitivity which could result in false negative results.
- Unclassified
Vehicle Recall · February 10, 2025
2024 HYUNDAI SANTA FE, 2025 HYUNDAI SANTA FEAn electrical short increases the risk of a fire.
- Class II
Medical Device Recall · February 10, 2025
Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05, 13894-16, 17550-08, 12236-18, 11854-15, 8043-29, 12466-17, 15599-1Customer-designed sterile surgical procedure packs contain latex components as specified; but, the content label sealed within the transparent sterile pouch contains the symbol for a latex-free product. If users or patients with latex sensitivity come into contact with latex, an allergic reaction may occur.
- Class II
Medical Device Recall · February 10, 2025
Origin Data Management software versions 3.1.0, 3.1.1, 3.1.2, 3.2.0, 3.2.1Under certain circumstances, it can occur that patient records from unrelated individuals are automatically merged into one patient record without user notification.
- Unclassified
Vehicle Recall · February 9, 2025
2024 KENWORTH T680, 2024 KENWORTH T880An instrument panel display that does not show critical information, such as warning lights or vehicle speed, increases the risk of a crash.
- Unclassified
Vehicle Recall · February 9, 2025
Mazda North American Operations
2025 MAZDA CX-90, 2025 MAZDA CX-70An inaccurate fuel gauge may result in the vehicle unexpectedly running out of fuel and stalling, increasing the risk of a crash.
- Class II
Food Recall · February 9, 2025
" Spinach Artichoke Dip (Sold Hot) 1 lb " Spinach Artichoke Dip (Sold Cold) 1 lb " Spinach Artichoke Dip (Sold in Bulk for Customer Self Service)Potential metal inclusion
- Class II
Medical Device Recall · February 7, 2025
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary oCatheter manufactured at the incorrect length.
- Class II
Drug Recall · February 7, 2025
Aspen Biopharma Labs Pvt., Ltd.
Chlorambucil Container Description: The product packed in double self-seal cover and finally packed in Aluminum cover for shipping.CGMP Deviations
- Class II
Medical Device Recall · February 7, 2025
Jinan Bodor Cnc Machine Co Ltd
Bodor's I series laser cutting machine.The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).
- Class II
Drug Recall · February 7, 2025
Aspen Biopharma Labs Pvt., Ltd.
Alprostadil Container Description: Amber color bottleCGMP Deviations
- Class II
Drug Recall · February 7, 2025
Aspen Biopharma Labs Pvt., Ltd.
Latanoprost NDC# 82187-1002-1 Container Description: Amber colour bottleCGMP Deviations
- Class II
Drug Recall · February 7, 2025
Aspen Biopharma Labs Pvt., Ltd.
Bimatoprost NDC# 82187-1001-1 Container description: The product packed in double self-seal cover and finally packed in Aluminum cover for shipping.CGMP Deviations
- Class III
Food Recall · February 7, 2025
LEMON PLUM; NET WT: 228G (8oz); INGREDIENTS: Plum, sugar, salt, lemon juice, food additives (citric acid, sodium benzoate, potassium sorbate, ethyl maltol, FD&C YELLOW#6, vanillin, saccharin sodium, sProduct contains cyclamates.
- Class I
Food Recall · February 7, 2025
Las Ollas Botana Mix snack, 2lbs, item #1516, # 1056, UPC# 880342001855Undeclared Sesame, Soy, Wheat, Yellow No. 5, Yellow No. 6, and Red No. 6.
- Unclassified
Vehicle Recall · February 7, 2025
2024 POLESTAR POLESTAR 2A loss of brake function increases the risk of a crash.
- Class II
Medical Device Recall · February 7, 2025
CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in the setting of an Electrophysiology or Catheterization Laboratory Model: 18-50Damage to the sterile barrier pouch of catheter, which could potentially compromise its sterility.
- Class II
Medical Device Recall · February 6, 2025
VEIN TRAY, Model No UTVT21C UTVT21C02 UTVT21C-03ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
NEURO IR TRAY , Model No WENI56JACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Drug Recall · February 6, 2025
SUN PHARMACEUTICAL INDUSTRIES INC
Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901. Distributed by: Sun Pharmaceutical Industries, Inc., CrFailed Dissolution Specifications
- Class II
Medical Device Recall · February 6, 2025
MAJOR DIEP, Model Nos. CCMJ73G-01 CCMJ73HACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
MAJOR VASCULAR PACK , Model No UTMV78X-01 UTMV78Y UTMV78Y-01 UTMV78X-01 UTMV78Y-02ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
LABOR & DELIVERY PACK, Model Nos LLLD19HACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
CENTRAL LINE PICC , Model No LLCL44H LLCL44H-01ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
URO ROBOTIC PACK , Model No LVUR44C LVUR44C-03ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
GENERAL ANGIO PACK , Model Nos LLAP75G LLAP75G-01 LLAP75G-02 LLAP75G-03ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
HIP SCOPE, Model Nos. CCHS21B CCHS21B-01 CCHS21B-02ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Unclassified
Consumer Product Recall · February 6, 2025
Jazwares LLC, of Sunrise, Florida
America's Got Talent microphonesThe lithium-ion batteries in the recalled microphones can overcharge and ignite, posing a fire hazard.
- Unclassified
Consumer Product Recall · February 6, 2025
LG Electronics Inc., of South Korea
Slide-In and Freestanding Electric RangesFront-mounted knobs on the recalled ranges can be activated by accidental contact by humans or pets, posing a fire hazard.
- Unclassified
Consumer Product Recall · February 6, 2025
Pella Corporation, of Pella, Iowa
Pella Reserve and Lifestyle Sliding Patio Doors and Lifestyle WindowsThe recalled products violate the mandatory federal regulations for consumer products containing button cell or coin batteries, because the sliding doors' sensor panel and the windows' remote control have button cell batteries that can be easily accessed by children. This poses an ingestion hazard. In addition, the recalled products do not have the required warnings. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- Class II
Medical Device Recall · February 6, 2025
DIAGNOSTIC NEURO IR TRAY , Model No WENE21ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
DELIVERY PACK , Model No SGDV22D-01 SGDV22EACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
OPEN HEART ADULT - SIDE A , Model Nos LLOH01I-01 LLOH01IACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
DR DIULUS INJECTION PACK, Model Nos. CCDU12C CCDU12D CCDU12D-01ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters, Medline Item Numbers: 401582R, 401904R, 401904R, 401905R, 401933R, and 401991RDevices may have higher than expected amounts of bacterial endotoxin.
- Class II
Medical Device Recall · February 6, 2025
LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07BACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
LAPAROSCOPY PACK , Model No SFLA02A SFLA02BACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
CYSTO , Model No SACY80RACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
CYSTO PACK , Model N. HKCY31AACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
LAPAROSCOPY PACK, Model Nos LLLA21J LLLA21J-02ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
BORN ON ARRIVAL KIT , Model No LLBN11BACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
LABOR & DELIVERY PPS , Model No LLLD64O LLLD64O-01 LLLD64O-02ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Drug Recall · February 6, 2025
Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton, Rx Only, For Topical Use Only, Manufactured by Padagis, Yeruham, Israel, NDC: 45802-0134-30Defective Container: Some packets may not be fully sealed, potentially allowing for loss of Ethanol from the product.
- Class II
Medical Device Recall · February 6, 2025
TOTAL HIP PACK , Model No SMTH06O SMTH06PACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
THORACIC PACK , Model No UTTC82Y UTTC82AA-01ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
AV FISTULA , Model No UTAV77TACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.