-
PERIPHERAL PARENTERAL NUTRITION, Compounded Sterile Preparation… recall
FDA
· Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles · Class II
-
Omeprazole Delayed-release Capsules, USP, 20mg, 1000-count bottle… recall
FDA
· Dr. Reddy's Laboratories, Inc. · Class II
-
Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 1000-count bottle… recall
FDA
· Accord Healthcare, Inc. · Class II
-
Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottle… recall
FDA
· Accord Healthcare, Inc. · Class II
-
Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 1000-count bottle… recall
FDA
· Accord Healthcare, Inc. · Class II
-
Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), 1000-count bottle… recall
FDA
· Accord Healthcare, Inc. · Class II
-
Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 90-count bottle… recall
FDA
· Accord Healthcare, Inc. · Class II
-
Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000-count bottle… recall
FDA
· Accord Healthcare, Inc. · Class II
-
Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 90-count bottle… recall
FDA
· Accord Healthcare, Inc. · Class II
-
Testosterone 200 mg Pellet packaged in 1mL amber vials, Rx only… recall
FDA
· Qualgen, LLC · Class III
-
Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottles… recall
FDA
· Sun Pharmaceutical Industries Inc · Class II
-
2024 Tiffin Convoy and 3 more recall: Alternator Controller Programming May Cause Engine Stall
NHTSA
· Tiffin Motorhomes, Inc.
-
2023–2025 Ferrari Purosangue recall: Loss of Braking Ability
NHTSA
· Ferrari North America, Inc.
-
2022–2024 BMW I4 and 5 more recall: Loss of Drive Power
NHTSA
· BMW of North America, LLC
-
2025 Winnebago Adventure Wagon and 7 more recall: Air Bags May Fail to Deploy
NHTSA
· Winnebago Industries, Inc.
-
2024–2025 Lamborghini Revuelto recall: Door Springs May Fail Unexpectedly
NHTSA
· Lamborghini (Automobili Lamborghini)
-
2020–2023 Nova BUS LFS recall: Steering Wheel May Turn Unintentionally
NHTSA
· Nova Bus (US) Inc.
-
Bestway, Intex, and Polygroup Recall Certain Above-Ground Pools 48 Inches and Taller Due to Drowning Hazard; Nine Deaths Reported…
CPSC
· Bestway, Intex, and Polygroup
-
2019–2022 Rosenbauer Avenger and 2 more recall: Odometer May Freeze
NHTSA
· Rosenbauer America
-
Bexco Enterprises Recalls Kiwi Electronic Recliner and Swivel Gliders with USB Port Due to Overheating Hazard
CPSC
· Bexco Enterprises
-
VIVI E-Bikes Lithium-ion Batteries Sold with VIVI E-Bikes Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death…
CPSC
· Guangzhou Plenty Bicycle Co., Ltd.
-
iStore Magnetic Wireless Power Banks Recalled Due to Fire and Burn Hazards; Imported by Tomauri
CPSC
· Tomauri Inc., of Ontario, Canada
-
Deale International Recalls CasaClean Handheld Steamers Due to Risk of Serious Burn Injury; Sold on HSN
CPSC
· Deale International
-
Primark Recalls DTR Stitch 4-pack Scented Highlighters Due to Risk of Phthalate Exposure; Violates Federal Phthalates Ban; Sold by Primark
CPSC
· Primark
-
Tractor Supply Recalls Traveller Aluminum Loading Ramps Due to Fall Hazard
CPSC
· Tractor Supply
-
2023–2025 Genesis G90 and 1 more recall: Instrument Panel Display Failure/FMVSS 101
NHTSA
· Hyundai Motor America
-
2025–2026 Grand Design Lineage recall: Door Entry Latch May Fail
NHTSA
· Grand Design RV, LLC
-
2023–2024 Jeep Grand Cherokee and 1 more recall: Head Restraints May Not Lock/FMVSS 202
NHTSA
· Chrysler (FCA US, LLC)
-
2024–2025 Chrysler Pacifica recall: Rearview Camera Image May Not Display/FMVSS 111
NHTSA
· Chrysler (FCA US, LLC)
-
Michelin Crossclimate 2 recall: Missing DOT Markings On Tire Sidewall/FMVSS 139
NHTSA
· Centropneus SRL
-
Mopar Head Restraint recall: Head Restraints May Not Lock
NHTSA
· Chrysler (FCA US, LLC)
-
Alcon Laboratories, Inc recall
FDA
· Alcon Research LLC · Class II
-
Alcon Laboratories, Inc recall
FDA
· Alcon Research LLC · Class II
-
Alcon Laboratories, Inc recall
FDA
· Alcon Research LLC · Class II
-
Preat, Astra EV-compatible 4.2mm Digital Analog recall
FDA
· Preat Corp · Class II
-
Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F… recall
FDA
· Boston Scientific Corporation · Class II
-
VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201… recall
FDA
· Boston Scientific Corporation · Class II
-
VersaCross RF Wire (VXW) recall
FDA
· Boston Scientific Corporation · Class II
-
VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J… recall
FDA
· Boston Scientific Corporation · Class II
-
O-arm O2 Imaging System recall
FDA
· Medtronic Navigation, Inc.-Boxborough · Class II
-
Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model recall
FDA
· Neurovision Medical Products Inc · Class II
-
Canturio¿ Smart Extension Product Name: CSE Implant Model recall
FDA
· Canary Medical, Inc. · Class II
-
Varicam, Millennium VG, Millennium VG Hawkeye… recall
FDA
· Ge Medical Systems Israel, Functional Imaging · Class II
-
Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye 4 Nuclear… recall
FDA
· Ge Medical Systems Israel, Functional Imaging · Class II
-
TrueDent White, TDM110, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Yellow, TDM140, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Magenta, TDM130, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Cyan, TDM 120, Model No recall
FDA
· Stratasys Ltd · Class III
-
TrueDent Clear, TDM 100, Model No recall
FDA
· Stratasys Ltd · Class III
-
FEM-FLEXII Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model recall
FDA
· Edwards Lifesciences, LLC · Class I
-
Bravo CF capsule delivery device, designed to place and attach a pH… recall
FDA
· Given Imaging Ltd. · Class I
-
Hillrom LikoScale component, Product Code 3156232… recall
FDA
· Baxter Healthcare Corporation · Class I
-
Hillrom Q-Link 13 component, Product Code 3156509… recall
FDA
· Baxter Healthcare Corporation · Class I
-
Crown Point Shelled Edamame, net wt recall
FDA
· Alpine Food DIstributing, Inc · Class II
-
Wegmans Semi-Sweet Chocolate Nonpareils, NET WT 18.5 OZ (1 LB 2.5 OZ) (524… recall
FDA
· Mellace Family Brands California Inc · Class II