Safety Recalls
RSS ↗15,379 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 13,101–13,150 of 15,379
- Class II
Medical Device Recall · March 20, 2024
Baxter Spectrum IQ Infusion Pump, Product Code 3570009One device was improperly performed testing prior to release from a Service Center.
- Class II
Medical Device Recall · March 20, 2024
ZPLP Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-017-08Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class I
Food Recall · March 20, 2024
Vanilla Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.Undeclared Allergen: milk, eggs, wheat, peanuts, and tree nuts.
- Class II
Medical Device Recall · March 20, 2024
ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 7-2357-018-04Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class II
Medical Device Recall · March 20, 2024
ZPLP Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Nonsterile-Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-08Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class II
Medical Device Recall · March 20, 2024
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractureThread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class II
Medical Device Recall · March 20, 2024
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fracturesThread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class I
Medical Device Recall · March 20, 2024
Dr¿ger Perseus A500 Anesthesia WorkstationUnexpected shutdown while operating on battery power.
- Class II
Medical Device Recall · March 20, 2024
Alinity m System, Part Number: 08N53-002The Alinity m System camera detects whether tubes are "capped." If the camera detects a cap and the retention bar is not present on the sample rack, the system will generate the message 'Error - 6013: Has cap, no retention bar." Abbott has identified an issue concerning the use of certain third-party Universal Transport Medium (UTM) tubes on the Alinity m System. This issue has been observed with Copan UTM-RT 3 mL Without Beads Transport & Preservation Medium for Viral Molecular Diagnostics Testing, Part Number (PN) 3C047N. However, it is possible that other third party manufactured tubes could experience the same issue.
- Class I
Food Recall · March 20, 2024
Peanut Butter Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.Undeclared Allergen: milk, eggs, wheat, peanuts, and tree nuts.
- Class II
Medical Device Recall · March 20, 2024
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fracturesThread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class I
Food Recall · March 20, 2024
Key Lime Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.Undeclared Allergen: milk, eggs, soy, wheat, peanuts, and tree nuts.
- Class II
Medical Device Recall · March 20, 2024
ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fracturesThread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class I
Food Recall · March 20, 2024
Raspberry Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.Undeclared Allergen: milk,eggs, wheat, peanuts, and tree nuts.
- Class II
Medical Device Recall · March 20, 2024
ZPLP Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-06Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class II
Medical Device Recall · March 20, 2024
ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-04Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class II
Medical Device Recall · March 20, 2024
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractureThread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class II
Medical Device Recall · March 20, 2024
ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fracturesThread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class II
Medical Device Recall · March 20, 2024
ZPLP Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Nonsterile-Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-10Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
- Class I
Drug Recall · March 19, 2024
GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural, UPC: N/A.Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula Blunt Tip, Model Number 30003Potential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Intracoronary Shunts: a) ClearView¿ 1.00 mm Intracoronary Shunt, Model Numbers: 31100; b) ClearView¿ 1.25 mm Intracoronary Shunt, Model Numbers: 31125; c) ClearView¿ 2.00 mm IntracoPotential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Left Heart Vent Catheters: a) DLP¿ Intracardiac Sump 20 Fr, Model Number 12012, b) DLP¿ Left Heart Vent Catheter 10 Fr., Model Number 12008, c) DLP¿ Left Heart Vent Catheter 13 Fr., MPotential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Cardioplegia Adapters: a) DLP¿ 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model Number 25009, b) DLP¿ 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model NumberPotential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Venous Cannulae: a) DLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120, b) DLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124, c) DLP¿ 28 Fr. MalPotential for unsealed sterile packing.
- Class I
Medical Device Recall · March 19, 2024
Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
- Class I
Medical Device Recall · March 19, 2024
Trilogy EV300, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
- Class I
Medical Device Recall · March 19, 2024
Garbin EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Aortic Root Cannulae and Cardioplegia Needles: a) DLP¿ 9 Ga (11 Fr) Aortic Root Cannula, Model Number 24009; b) DLP¿ 16 Ga (5 Fr) Cardioplegia Needle Neonatal 0.64 cm (1/4 in) Tip LePotential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx OnlyNail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Disposable Pressure Display Sets: a) DLP¿ 114.3 cm (45 in), Model Number 61000; b) DLP¿ 114.3 cm (45 in), Model Number 62000Potential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001Potential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Suction Tubes: a) DLP¿ Suction Tube 6-Fr. Shaft with Frazier Tip, Model Number: 10050, b) DLP¿ Suction Tube 6-Fr. Shaft with 10-Fr. Soft Tip, Model Number: 10052, c) DLP¿ Suction TubPotential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx OnlyNail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Arterial Cannulae packaged as: a) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020; b) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220; c) DLP¿ CurvPotential for unsealed sterile packing.
- Class I
Drug Recall · March 19, 2024
Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
Spanish Fly 22K capsules, 2-count box, UPC 0 664979 979455Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
Samurai-X Honey 6800, UPC 2 56891 27553 3.Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
HONEY MANUKA BUNNY LOVE, 12g, All Natural Sexual Enhancement, UPC: N/AMarketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
ALPHASTRIP MALE PERFORMANCE ENHANCER, The fastest acting sublingual, Serving Size (1 strip), Distributed by: GALT INT'LMarketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
SILVERBACK XXX POWER MALE ENHANCEMENT, 2 fl. oz., UPC 8 700470 032762Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Medical Device Recall · March 19, 2024
Trilogy Evo, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
- Class I
Drug Recall · March 19, 2024
libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box, UPC 7 05105 83073 5.Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
The GOAT SUBLINGUAL STRIP, MALE ENHANCEMENT, 2 Pack, Distributed by Hombres LLC, 130 Maccormick Ave, Suite 105, Costa Mesa, A, UPC 6 61631 26363 1.Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
Flower Power, CBD infused Female Enhancement, 59 ml bottle, UPC 0 678741 351646.Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class I
Drug Recall · March 19, 2024
Weiner Boner Honey, 12g packet, 100% Organic Formula.Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
- Class II
Medical Device Recall · March 19, 2024
Medtronic Tourniquet Sets: a) DLP¿ 5.5 in (14.0 cm) Tourniquet Kit, Model Number 79004, b) DLP¿ 7 in (17.8 cm) Tourniquet Kit, Model Number 79009Potential for unsealed sterile packing.
- Class II
Medical Device Recall · March 19, 2024
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050Potential for unsealed sterile packing.
- Class I
Medical Device Recall · March 19, 2024
LifeVentEVO2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
- Class I
Medical Device Recall · March 19, 2024
Aeris EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.