Safety Recalls

17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 751–800 of 17,395

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  ConMed Corporation

  CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures Sterile

  Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.

  Class II

• Drug Recall · July 14, 2026

  Precision Dose Inc.

  Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080, unit-dose oral syringes, NDCs 68094-073-01 (oral syringe) and 68094-073-58 (case).

  Failed Impurities/Degradation Specifications

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Medical Device Recall · July 14, 2026

  Fresenius Medical Care Renal Therapies Group, LLC

  Citrasate, Liquid Acid Concentrate for Bicarbonate Hemodialysis: Product Numbers: 08-2251-CA, 08-3251-CA, 13-2251-CA; Liquid Acid Concentrate for Bicarbonate Hemodialysis

  Complaints of blue-green discoloration in product

  Class II

• Medical Device Recall · July 14, 2026

  Boston Scientific Corporation

  Suture Cinch Long 1pk. Endoscopic tissue approximation device.

  Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Digi Eye (hypromellose 0.35%, tetrahydrozoline HCl 0.05%), Sterile, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Cardinal Health 200, LLC

  Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO , Cata

  Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

  Class II

• Drug Recall · July 14, 2026

  Rohto-Mentholatum (Vietnam) Co., Ltd.

  Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 80 0.2%), Sterile, TWIN PACK, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Mad

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · July 14, 2026

  Fresenius Medical Care Renal Therapies Group, LLC

  GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B; 0FD3251-3B; Dry Acid Concentrate for Bicarbonate Hemodialysis

  Complaints of blue-green discoloration in product

  Class II

• Food Recall · July 13, 2026

  KHONG GUAN (HQ)

  BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000084

  Undeclared peanuts.

  Class I

• Medical Device Recall · July 13, 2026

  Medtronic MiniMed, Inc.

  MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW

  Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

  Class II

• Medical Device Recall · July 13, 2026

  OBP Medical Corporation

  OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

  There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.

  Class II

• Medical Device Recall · July 13, 2026

  Siemens Healthcare Diagnostics, Inc.

  Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL, 1x14mL

  Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk of sub-optimal patient treatment, including potential life-threatening cardiac arrhythmias or inadequate antimalarial therapy.

  Class II

• Medical Device Recall · July 13, 2026

  Medline Industries, LP

  Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product Number/SKU 780-07); 2) HUDSON RCI, DBM-CIRCUIT,VENT,NEONAT

  Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage. Device failure may predispose infant to bronchospasm, inspissated secretions, and airway obstruction, as well as inadvertent positive end-expiratory pressure (PEEP), circuit obstruction, or accidental lavage of pooled fluid into the airway, elevated oxygen consumption, and worsening respiratory distress.

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Dist

  Subpotent Drug

  Class II

• Medical Device Recall · July 13, 2026

  Medline Industries, LP

  Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI, CIRCUIT, NEO, SING LIMB, HTD,COLUMN, Medline Product Number/SKU HUD78001KIT (Teleflex Product Number/SKU 780-01KIT); 2) MEDLINE HUDSO

  Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage. Device failure may predispose infant to bronchospasm, inspissated secretions, and airway obstruction, as well as inadvertent positive end-expiratory pressure (PEEP), circuit obstruction, or accidental lavage of pooled fluid into the airway, elevated oxygen consumption, and worsening respiratory distress.

  Class II

• Medical Device Recall · July 13, 2026

  Siemens Healthcare Diagnostics Products Ltd.

  Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF:L2KSY2(D)/10471981 IVD, RxOnly

  Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distri

  Subpotent Drug

  Class II

• Medical Device Recall · July 13, 2026

  Gentherm Medical, LLC

  Blanketrol III, Model 233; Thermal regulating system.

  Overheating of the 115V CPU board may cause the device to shut down.

  Class II

• Medical Device Recall · July 13, 2026

  Straumann USA LLC

  GM Helix Implant, Endosseous Dental Implant Article No. 109.984

  There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue could cause bone compression or difficulty during installation in situations where there is sufficient bone volume

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Medical Device Recall · July 13, 2026

  Medtronic MiniMed, Inc.

  MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;

  Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

  Class II

• Medical Device Recall · July 13, 2026

  Gentherm Medical, LLC

  Innercool Coolblue Console, Model STx; Thermal regulating system.

  Overheating of the 115V CPU board may cause the device to shut down.

  Class II

• Medical Device Recall · July 13, 2026

  Medtronic MiniMed, Inc.

  MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;

  Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

  Class II

• Medical Device Recall · July 13, 2026

  Siemens Healthcare Diagnostics, Inc.

  Beckman Coulter, Emit 2000 Quinidine Assay REF: OSR4Q229 Contents: R1: 2 x 23 mL;R2 2x13 mL

  Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk of sub-optimal patient treatment, including potential life-threatening cardiac arrhythmias or inadequate antimalarial therapy.

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distri

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Dist

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Rising Pharma Holding, Inc.

  Rising, Cyproheptadine Hydrochloride Syrup, 2mg/5 mL, 473 mL (ONE PINT), Rx only, Manufactured for: Rising Pharma Holdings, Inc., East Brunswick, NJ, Manufactured by: Lyne Laboratories, Inc., Brockton

  Presence of Precipitate: medication was crystallizing and particles floating in the bottle

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. N

  Subpotent Drug

  Class II

• Food Recall · July 13, 2026

  PT Organics Limited

  Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720. Distributed by: PT Organics Ltd, 333 South State St, Suite V-142, Lake Oswego, OR

  Possible foreign object (thin, soft plastic strands).

  Class II

• Food Recall · July 13, 2026

  KHONG GUAN (HQ)

  Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053

  Undeclared peanuts.

  Class I

• Medical Device Recall · July 13, 2026

  Siemens Healthcare Diagnostics Products Ltd.

  Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF(s):L2kSY2/10489085; L2KSY6/10488319 IVD, RxOnly

  Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC

  Subpotent Drug

  Class II

• Medical Device Recall · July 13, 2026

  Gentherm Medical, LLC

  Blanketrol II Model 222S; Thermal regulating system.

  Overheating of the 115V CPU board may cause the device to shut down.

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distri

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 112 mcg (0.0112 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. N

  Subpotent Drug

  Class II

• Drug Recall · July 13, 2026

  Major Pharmaceuticals

  Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. N

  Subpotent Drug

  Class II

• Medical Device Recall · July 13, 2026

  Kico Knee Innovation Company

  Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200 Software Version: ARVIS Hip and Knee Gap Balance Software v3.3.2 (IN-28200) ARV

  Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing

  Class II

• Medical Device Recall · July 13, 2026

  Medline Industries, LP

  Medline Hudson RCI, DBD-CIRCUIT,VENT,INSPIRATORY,HEATED,NEO, Medline Product Number/SKU HUD78019 (Teleflex Product Number/SKU 780-19); breathing circuit. Respiratory gas humidifier.

  Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage. Device failure may predispose infant to bronchospasm, inspissated secretions, and airway obstruction, as well as inadvertent positive end-expiratory pressure (PEEP), circuit obstruction, or accidental lavage of pooled fluid into the airway, elevated oxygen consumption, and worsening respiratory distress.

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330

  Component labeling discrepancy

  Class II

• Medical Device Recall · July 10, 2026

  Paragon 28, Inc.

  Custom Made Device Implant 6123 Navicular Cage Small Right Rev A, Model/Catalog Number 6123S R; foot implant

  Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

  Class III

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) FEMORAL PACK, Medline Kit SKU DYNJ909393A; 2) FEVAR, Medline Kit SKU DYNJ910295D.

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) LAVH, Medline Kit SKU CDS982273U; 2) GYN ABDOMINAL CDS, Medline Kit SKU CDS982654L; 3) GYN LAP HYSTERECTOMY CDS, Medline Kit SKU CDS982662Q; 4) CMH VAG

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Medline Kit SKU DYNJ900957C; 3) GYN LAPAROTOMY, Medline Kit SKU DYNJ906804B

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Medline Industries, LP

  Medline convenience kits labeled as: 1) GYN ROBOTIC CDS, Medline Kit SKU CDS982888Q; 2) GYN ROBOTIC ADD ON PACK, Medline Kit SKU DYNJ43837D; 3) OH GYN/LAP ROBOT PACK, Medline Kit SKU DYNJ89759;

  Kits contain a potentially contaminated component which were recalled by the manufacturer

  Class II

• Medical Device Recall · July 10, 2026

  Paragon 28, Inc.

  Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A, Model/Catalog Number 6123N R; foot implant

  Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

  Class III