Medline is recalling convenience kits containing select 10mL polycarbonate syringes due to potential cracking or breakage of the syringe barrel and/or plunger, which could result in loss of sterility and potential patient infection.
21 products
Magellan recalls LeadCare II blood lead test kits over false elevated results from certain micro-collection devices.
4 products
Integra LifeSciences is recalling CUSA Clarity C7000 Console (Software 2.1.1.909) due to unresponsive touch screen.
Angiodynamics recalls Soft-Vu Angiographic Catheters due to guidewire passage defect.
20 products
Windstone recalls kits with Medline Namic RA Syringes over risk of adapter unwinding, which may cause disconnection and serious injury.
Apotex is recalling Desmopressin Nasal Spray (NDC 60505-0815-0) due to defective bottle caps with missing or dislodged liners.
3 products
Medline is recalling CENTURION Circumcision Kit (CIT7050F) due to one lot distributed without sterilization.
Philips Spectral CT on Rails (Model 728334) requires a software update to address gantry positioning, message display, and menu option issues.
International Medication Systems is recalling Epinephrine Injection 1 mg/10mL (NDC 76329-3318-1) due to lack of sterility assurance.
Cytal Wound Matrix 2-Layer 5x5 cm recalled over out-of-specification endotoxin results.
5 products
React Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.
B. Braun recalls STREAMLINE bloodline sets for Dialog DR over arterial line air bubble risk.
6 products
Clariance-SAS is recalling Elegance Anterior Cervical Plates due to the presence of burrs on the finished product.
2 products
Huons recalls injectable lidocaine, bupivacaine, and saline due to sterility concerns.
9 products
Island Kinetics recalls hydrocortisone 1% gels (Remedy Gel, Skin Rehab, Essential Calming) due to subpotency.
3 products
Nephron SC recalling Albuterol Sulfate Inhalation Solution (NDC 69374-330-05) due to illegible labeling.
Taro recalls Fluocinonide 0.05% Cream 15g tubes due to out-of-spec viscosity.
3 products
Wilson-Cook Medical is recalling the Instinct Plus Endoscopic Clipping Device due to a potential for the device to malfunction.
HydroPeptide Clear Alliance Serum recalled due to benzene contamination.
4 products
Cipla recalls Cinacalcet HCl 30 mg tablets over N-Nitroso impurity above acceptable limit.
3 products
Exchange Select Honey Lemon Cough Drops recalled over quality concerns from FDA inspection.
15 products
Remel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing results.
LinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.
Philips is recalling AneurysmFlow software because the MAFA ratio provides unreliable prognostic data for aneurysm treatment decisions.
Arjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.
Cipla recalls Lanreotide Injection 120 mg/0.5 mL over sterility assurance concerns.
2 products
GE Healthcare recalls Omnipaque (iohexol) Injection 350 mg/mL due to particulate matter.
2 products
Stryker is recalling tourniquet cuffs that may detach from the bladder, preventing the device from maintaining pressure.
Blaine Labs recalls multiple topical antiseptic/antifungal gels and creams due to Lysinibacillus fusiformis contamination.
9 products
Imu-Tek recalls Colostrum-5 capsules and powder due to under-processing.
2 products
Divided Sunset Multi Collagen Peptides are recalled for failing to declare egg and fish allergens on the product label.
Viatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
Teva is recalling 40 mg Isotretinoin Capsules due to potency issues.
2 products
Fagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.
5 products
Geri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.
Medline recalls convenience kits with Namic RA syringes over risk of loose connection or disconnection during use.
25 products
Siemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.
Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
Fresenius Kabi recalls 14 lots of Sodium Chloride and Dextrose Injections due to sterility concerns.
14 products
Tornier is recalling shoulder system components incorrectly labeled as HRS Max parts, as they are incompatible with the HRS Max system.
Medline is recalling Anterior Hip Packs containing Olympus biopsy valves over risk of rubber fragment detachment.
8 products
GE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
Medtronic MiniMed recalls all Paradigm, 600, and BLE 700 series insulin pumps over insulin delivery errors that can cause severe hypoglycemia or ketoacidosis.
14 products
Burlington Medical wrap aprons may lose shielding effectiveness over time.
13 products
Oxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products
Cardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
American Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
Merit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products