Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,751–7,800 of 15,271
- Class II
Medical Device Recall · February 25, 2025
Nasopore FD fragmentable nasal dressing, Catalog Numbers 5400-020-108 and 5400-020-108ITLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
- Class II
Medical Device Recall · February 25, 2025
Baxter Floor mounting column TruSystem 7500, Product Code 1717021There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
- Class II
Medical Device Recall · February 25, 2025
Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
- Class II
Medical Device Recall · February 25, 2025
Otopore Square outer ear wound dressing, Firm Catalog Number 5400-020-100 and Forte Catalog Number 5400-020-100ITLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
- Class II
Medical Device Recall · February 25, 2025
Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Number 5400-020-000TLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Hemopore 8cm nasal/sinus temporary wound dressing, Catalog Numbers 5400-020-208 and 5400-020-208ITL (OUS)There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth toA wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
- Class II
Medical Device Recall · February 25, 2025
Baxter Mobile column TruSystem 7500 U, Product Code 1730720There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
- Class II
Medical Device Recall · February 25, 2025
Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birthA wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
- Class II
Medical Device Recall · February 25, 2025
Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth tA wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
- Class II
Medical Device Recall · February 25, 2025
Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
- Class II
Medical Device Recall · February 25, 2025
Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
- Class II
Medical Device Recall · February 25, 2025
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004SThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Nasopore Ex Firm 4cm fragmentable nasal dressing, Catalog Number 5400-030-004 and Nasopore Forte plus 4cm Catalog Number 5400-030-004ITLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Nasopore Ex Firm 8cm fragmentable nasal dressing, Catalog Number 5400-030-008 and Nasopore Forte plus 8cm Catalog Number 5400-030-008ITLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 25, 2025
Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITLThere is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- Class II
Medical Device Recall · February 24, 2025
Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraoperative Lead, Medium Model/Catalog Number: REF# 9525 (Medium) Product Description: The Checkpoint GuardiAdhesive on the back of the lead may not fully encapsulate the metallic portion of the wire and button subassembly, potentially leading to exposed metal. There is a risk of electrical current leakage, which may lead to inconsistent or confusing muscle responses, potentially compromising the effectiveness of the intended use as the surgeon could take an incorrect clinical action.
- Class II
Medical Device Recall · February 24, 2025
Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraoperative Lead, Small Model/Catalog Number: REF# 9524 (Small) Product Description: The Checkpoint GuardianAdhesive on the back of the lead may not fully encapsulate the metallic portion of the wire and button subassembly, potentially leading to exposed metal. There is a risk of electrical current leakage, which may lead to inconsistent or confusing muscle responses, potentially compromising the effectiveness of the intended use as the surgeon could take an incorrect clinical action.
- Class I
Medical Device Recall · February 24, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C; 2) NEWBORN RESUSCITATION KIT, REF ACC010381A; 3) NEWBORN RESUSCITATION KIT, REF ACC010381B; 4) NEWBORSpecific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.
- Class II
Medical Device Recall · February 24, 2025
DePuy Mitek, Inc., a Johnson & Johnson Co.
COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.Device is missing the pin in the graft loader component.
- Class III
Drug Recall · February 24, 2025
Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5 mL fill in 15 mL bottle, Imprimis NJOF, LLC, Route 46 West, Unit 6B, Ledgewood, NJ, 07852, NDSub-Potent Drug: The stability batch showed a subpotent result, which does not meet the product specifications of 90.0-110.0% of the label claim.
- Class III
Drug Recall · February 24, 2025
Livalo (pitavatstatin) tablets, 4 mg, 90-count bottles, Rx only, Manufactured by: Patheon, Inc. Cincinnati, OH 45237 USA or by Kowa Company, Ltd, Nagoya, 462-0024 Japan, Marketed by Kowa PharmaceuticaPresence of foreign tablets/capsules
- Class II
Drug Recall · February 24, 2025
Zapzyt, Acne Treatment Gel, 10% benzoyl peroxide Gel, packaged in 1 oz (28.35g) tube, Distributed by: FOCUS CONSUMER HEALTHCARE, LLC., 801 Broad St Ste 200, Chattanooga, TN 37402. NDC 71687-0011-1Chemical Contamination: Presence of benzene.
- Class II
Medical Device Recall · February 24, 2025
DePuy Mitek, Inc., a Johnson & Johnson Co.
COR Disposable Kit, 8 mm. Cartilage Transplant System.Device is missing the pin in the graft loader component.
- Class II
Medical Device Recall · February 24, 2025
Boppli: Bedside Device Kit, REF: 54-0002; Sensor Band, REF: 51-0007Single-use battery-powered blood pressure monitor, for use on neonates and infants, due to vibratory noise, may not adequately detect changes in blood pressure per specification. Containment actions: 1) Ventilator lines not to touch the isolette (e.g. mattress, side rails, pillow) or patient, 2) Move affected monitor to patient's foot.
- Class II
Food Recall · February 23, 2025
Chocolate Peanut Butter Protein Balls. Product has expected life of 2 weeks and does not require refrigeration. Product is packaged in sets of 2 protein balls into resealable plastic baggies. Net Wt.Undeclared soy lecithin and undeclared color additives Blue 1 Lake, Yellow 6, Red 40, Yellow 5, Blue 1, Yellow 6 Lake, Red 40 Lake, Yellow 5 Lake, Blue 2 Lake, Blue 2.
- Class II
Food Recall · February 21, 2025
CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 946 mL UPC 0 41271 01993 3 Distributed by: Danone US, LLCThe firm received complaints of spoilage and illness with the use of the products.
- Class I
Food Recall · February 21, 2025
Ready Care Vanilla Shake (4 oz), UPC 10045796017334; Imperial Vanilla Shake (4 oz), UPC 00074865926836Potential contamination with Listeria monocytogenes.
- Class I
Food Recall · February 21, 2025
Ready Care Chocolate Shake (4 oz), UPC 10045796017341; Imperial Chocolate Shake (4 oz), UPC 00074865926997Potential contamination with Listeria monocytogenes.
- Class I
Food Recall · February 21, 2025
Ready Care Strawberry Shake No Sugar Added (4 oz), UPC 10045796017372; Imperial Strawberry Shake No Sugar Added (4 oz), UPC 00074865926843Potential contamination with Listeria monocytogenes.
- Class I
Food Recall · February 21, 2025
Ready Care Chocolate Shake Plus (4 oz), UPC 10045796017471Potential contamination with Listeria monocytogenes.
- Class I
Food Recall · February 21, 2025
Ready Care Vanilla Shake Plus (4 oz), UPC 10045796017549Potential contamination with Listeria monocytogenes.
- Class I
Food Recall · February 21, 2025
Ready Care Strawberry Banana Shake No Sugar Added (4 oz), UPC 10045796018447; Imperial Strawberry Banana Shake No Sugar Added (4 oz), UPC 00074865987325Potential contamination with Listeria monocytogenes.
- Class II
Food Recall · February 21, 2025
1.) Market Pantry Soup & Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case, Distributed By: Target Corporation, Minneapolis, MN 55403 2.) Great Value Soup & OPotential foreign material (stainless steel wire)
- Class I
Food Recall · February 21, 2025
Ready Care Strawberry Shake (4 oz), UPC 10045796017358; Imperial Strawberry Shake (4 oz), UPC 00074865927017Potential contamination with Listeria monocytogenes.
- Class I
Medical Device Recall · February 21, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CPB ADJUNCT PACK, DR. C PACK, PK CUST CV A&B C CO, TOL DR R PACK, TOL DR. C PACK, TOL DR. M PACK.Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
- Class I
Medical Device Recall · February 21, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LFMedical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
- Class I
Medical Device Recall · February 21, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK,Medline medical procedure kits, containing Medtronic Aortic Root Cannula
- Class I
Food Recall · February 21, 2025
Ready Care Strawberry Shake Plus (4 oz), UPC 10045796017495Potential contamination with Listeria monocytogenes.
- Class I
Food Recall · February 21, 2025
Ready Care Chocolate Shake No Sugar Added (4 oz), UPC 10045796036335; Imperial Chocolate Shake No Sugar Added (4 oz), UPC 10734730244720Potential contamination with Listeria monocytogenes.
- Class II
Food Recall · February 21, 2025
HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 32 FL OZ (1 QT) 946 mL UPC 0 41271 02565 2 Distributed by: Danone US, LLCThe firm received complaints of spoilage and illness with the use of the products.
- Class I
Food Recall · February 21, 2025
Ready Care Vanilla Shake No Sugar Added (4 oz), UPC 10045796017365; Imperial Vanilla Shake No Sugar Added (4 oz), UPC 00074865927031Potential contamination with Listeria monocytogenes.
- Class I
Medical Device Recall · February 21, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: TOL DR R PACKMedical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
- Class II
Medical Device Recall · February 20, 2025
IVX Station Reconstitution Transfer Set. Model Number: 298921215. Packaging: 1 set per White Tyvek Pouch, 5 Tyvek Pouches per shelf box, 10 shelf boxes per case box. IVX Station Reconstitution TranIVX Station Reconstitution Transfer Sets were shipped in advance of the IVX Station upgrade and not intended for clinical use but are engineering devices intended for use during set up and system calibration. The items were not shipped in a validated packing configuration and sterility cannot be ensured.
- Class II
Medical Device Recall · February 20, 2025
Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade titanium alloy: (1) REF 82-3300SP, 33mm W x 24mm D x 10mm H, 7 degrees; (2) REF 82-3700SP, 37mmThe product is mislabeled with the incorrect anterior height of 10mm, but the laser marking on the implant and corresponding trial both show the correct anterior height of 10.5mm.
- Class II
Medical Device Recall · February 20, 2025
Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory Syncytial Virus, Multi-analyte, unassayed quality control material, Catalog Number HE0044NThe RSV target may give a late Ct value and could potentially not pass QC.