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Consumer Product Recalls

127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.

January 15, 2025DrugsFDA
Eugia US LLC recalls medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL, Rx only, 1 mL Single-Dose Vial, Mfd in India for:
Hazard: CGMP Deviations
January 15, 2025DrugsFDA
Amerisource Health Services LLC recalls Clobazam Tablets, 10 mg, packaged in 30 tablets per carton (3x10 blister cards each), Rx Only, Amneal Pharmaceuticals LL
Hazard: Presence of Foreign Tablets/Capsules
January 15, 2025DrugsFDA
West-Ward Columbus Inc recalls Methadone Hydrochloride Tablets, USP, 5mg, 10x10 Unit-Dose Tablets, Rx Only, Distributed by: Hikma Pharmaceuticals USA I
Hazard: Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
January 15, 2025DrugsFDA
FDC Limited recalls Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, Sterile, package in 5 mL bottles, Rx Only, Distributed by: Leading
Hazard: Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
January 15, 2025DrugsFDA
Endo USA, Inc. recalls Clonazepam Orally Disintegrating Tablets, USP, 1 mg, C-IV, Rx Only, 60 tablets per carton (10 blister cards containing 6
Hazard: Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
January 15, 2025DrugsFDA
Endo USA, Inc. recalls Clonazepam Orally Disintegrating Tablets, USP, 0.25 mg, C-IV, Rx Only, 60 tablets per carton (10 blister cards containin
Hazard: Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
January 15, 2025DrugsFDA
Endo USA, Inc. recalls Clonazepam Orally Disintegrating Tablets, USP, 0.125 mg, C-IV, Rx Only, 60 tablets per carton (10 blister cards containi
Hazard: Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
January 15, 2025DrugsFDA
Endo USA, Inc. recalls Clonazepam Orally Disintegrating Tablet, USP, 2 mg, C-IV, Rx Only, 60 Tablets per carton, 10 blister cards containing 6
Hazard: Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
January 15, 2025DrugsFDA
Buy-Herbal recalls Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang,
Hazard: Marketed without an Approved NDA/ANDA: FDA analysis found the products to be tainted with undeclared Furosemide, Dexamethasone and Chlorpheniramine
January 15, 2025VehiclesNHTSA
Marion Body Works 2024 Equipment recall
Hazard: Overextension of the cab tilt cylinder can cause the cab to drop, increasing the risk of injury.
January 14, 2025VehiclesNHTSA
Palfinger 2017–2025 Exterior Lighting recall
Hazard: Incorrectly positioned lights can reduce the vehicle's visibility to other drivers, increasing the risk of a crash.
January 14, 2025Vehicle EquipmentNHTSA
GKN Aftermarket Power Train recall
Hazard: A cracked or broken driveshaft can cause a loss of drive power or a vehicle rollaway while in Park. Both scenarios increase the risk of a crash.
January 13, 2025VehiclesNHTSA
Winnebago 2025 Equipment recall
Hazard: A detached spare tire carrier can become a road hazard, increasing the risk of a crash.
January 13, 2025VehiclesNHTSA
KIA 2024–2025 Exterior Lighting recall
Hazard: A loss of headlights and taillights can reduce visibility, increasing the risk of a crash.
January 13, 2025VehiclesNHTSA
Forest River 2025 Equipment recall
Hazard: A gas leak in the presence of an ignition source can increase the risk of a fire.
January 13, 2025Vehicle EquipmentNHTSA
Nivion Electrical System recall
Hazard: Inadequate clearance between DC busbars may cause electrical arcing, increasing the risk of a fire. Additionally, disconnecting the adaptor during charging increases the risk of injury by electrical shock.
January 8, 2025Medical DevicesFDA
Carwild Corporation recalls Ivalon Anatomical Nasal Packing with Airway Tube and String, 8.0 cm x 1.5cmx 3.0 cm- Intended To Be Used During Ophthalm
Hazard: Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
January 8, 2025Medical DevicesFDA
Carwild Corporation recalls Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During Ophthalmic Surgical Procedures For Fluid Management Mode
Hazard: Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
January 8, 2025Medical DevicesFDA
Carwild Corporation recalls Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site.
Hazard: Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
January 8, 2025Medical DevicesFDA
3M Unitek Corporation recalls 3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self E
Hazard: Due to an increase of complaints for bracket bond failures and skin irritation or blistering.
January 8, 2025Medical DevicesFDA
Med Michigan Holding Llc recalls SUC-4300S, Rigid Intracardiac Sucker Fluted Tip; 1/4" (6.4mm) connector 13" (33cm) length. Indicated for handheld use on
Hazard: Incomplete or partial pouch seals, which may result in a breach in the sterility.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) CRANI, REF CDS780089V; 2) CRANIOFACIAL CDS, REF CDS780102K; 3)
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF, REF DYNJ0867145G; 2) CERVICAL SPINE PACK HUM
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DY
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls See DocMan
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK, REF DYNJ80585A; 2) MICRODISECTOMY PACK, R
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls See DocMan
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF D
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, REF DYNJ0660040R; 2) FREE FLAP PACK-
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.