Vereinigte Staaten Recalls

Verbraucherrückrufe von FDA, CPSC, NHTSA und USDA FSIS.

Showing 24 of 17,563 results
Medical DeviceUSFDA Devices

IQon Spectral CT; Product Code (REF): 728332;

Philips North America Llc
FDA DevicesClass II

IQon Spectral CT; Product Code (REF): 728332;

As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.

Feb 18, 2026Philips North America Llc
Medical DeviceUSFDA Devices

Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109

Medline Industries, LP
FDA DevicesClass II

Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Feb 18, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM

Straumann USA LLC
FDA DevicesClass III

WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM

The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.

Feb 18, 2026Straumann USA LLC
Medical DeviceUSFDA Devices

1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit SKU DYNDC3107; 8) NON STERILE DIALYSIS KIT, Kit SKU DYNDH1029C; 9) UMBILICAL TRAY W/3.5&5FR CATH, Kit SKU UVT1250; 10) UMBILICAL VESSEL TRAY, Kit SKU UVT835; 11) HEMODIALYSIS TRAY, Kit SKU VAR101HVAA.

Medline Industries, LP
FDA DevicesClass II

1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit SKU DYNDC3107; 8) NON STERILE DIALYSIS KIT, Kit SKU DYNDH1029C; 9) UMBILICAL TRAY W/3.5&5FR CATH, Kit SKU UVT1250; 10) UMBILICAL VESSEL TRAY, Kit SKU UVT835; 11) HEMODIALYSIS TRAY, Kit SKU VAR101HVAA.

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Feb 18, 2026Medline Industries, LP
PharmaceuticalUSFDA Drugs

UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041 Arco Corporate Drive, Suite 200, Raleigh, NC 27617, NDC 69448-025-63

McKesson
FDA DrugsClass I

UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041 Arco Corporate Drive, Suite 200, Raleigh, NC 27617, NDC 69448-025-63

Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.

Feb 18, 2026McKesson
Medical DeviceUSFDA Devices

Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

Feb 18, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PharmaceuticalUSFDA Drugs

Testosterone 100mg, Anastrozole 4mg (4.5), 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-01.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

Testosterone 100mg, Anastrozole 4mg (4.5), 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-01.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
Medical DeviceUSFDA Devices

Spectral CT 7500 on Rails; Product Code (REF): 728334;

Philips North America Llc
FDA DevicesClass II

Spectral CT 7500 on Rails; Product Code (REF): 728334;

As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.

Feb 18, 2026Philips North America Llc
Medical DeviceUSFDA Devices

Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X

Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

Feb 18, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PharmaceuticalUSFDA Drugs

Testosterone, 25.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1025-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

Testosterone, 25.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1025-32.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
PharmaceuticalUSFDA Drugs

Testosterone, 62.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1062-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

Testosterone, 62.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1062-32.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
PharmaceuticalUSFDA Drugs

Testosterone 87.5mg, Triamcinolone Acetonide17.5 mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-6087-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

Testosterone 87.5mg, Triamcinolone Acetonide17.5 mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-6087-32.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
PharmaceuticalUSFDA Drugs

Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-112-11

Pro Numb Tattoo Numbing Spray LLC
FDA DrugsClass II

Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-112-11

cGMP deviations

Feb 18, 2026Pro Numb Tattoo Numbing Spray LLC
PharmaceuticalUSFDA Drugs

Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-32

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-32

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
Medical DeviceUSFDA Devices

Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH ACUSON AcuNav Ultrasound Catheter, Use on Siemens Systems 10135936RH, 08255790RH

Medline Industries, LP
FDA DevicesClass I

Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH ACUSON AcuNav Ultrasound Catheter, Use on Siemens Systems 10135936RH, 08255790RH

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Feb 18, 2026Medline Industries, LP
PharmaceuticalUSFDA Drugs

acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, For Intravenous Use, Single-Use Bag, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-035-56

Fresenius Kabi Compounding, LLC
FDA DrugsClass II

acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, For Intravenous Use, Single-Use Bag, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-035-56

Lack of Assurance of Sterility

Feb 18, 2026Fresenius Kabi Compounding, LLC
PharmaceuticalUSFDA Drugs

ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride Injection, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-050-56

Fresenius Kabi Compounding, LLC
FDA DrugsClass II

ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride Injection, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-050-56

Lack of Assurance of Sterility

Feb 18, 2026Fresenius Kabi Compounding, LLC
Medical DeviceUSFDA Devices

Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81483RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81102RH 81104RH 81174RH 81531RH 81532RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 5mm 81107RH; Inquiry Steerable Diagnostic Catheter 4 Elec. 2-5-2mm 81402RH 81404RH 81405RH 81474RH; Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81473RH

Medline Industries, LP
FDA DevicesClass I

Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81483RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81102RH 81104RH 81174RH 81531RH 81532RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 5mm 81107RH; Inquiry Steerable Diagnostic Catheter 4 Elec. 2-5-2mm 81402RH 81404RH 81405RH 81474RH; Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81473RH

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Feb 18, 2026Medline Industries, LP
PharmaceuticalUSFDA Drugs

ESTRADIOL, 18 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 3521, NDC: 79559-3018-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

ESTRADIOL, 18 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 3521, NDC: 79559-3018-32.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
Food & BeverageUSFDA Food

CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET WT 0.75OZ DIST BY: DYMA BRANDS, INC. ATLANTA, GA 30328; Product also sold under the following brand names: FLAVOR Fresh PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY: DYMA BRANDS, INC. ATLANTA, GA 30328; HOUSE RECIPE CREAMY PEANUT BUTTER NET WT 0.75 OZ (21.2g) DISTRIBUTED BY SYSCO COROPRATION, HOUSTON, TEXAS 77077; Katy's Kitchen SMOOTH PEANUT BUTTER NET WT 0.75 OZ (21g) MARKETED BY INDEPENDENT MARKETING ALLIANCE HOUSTIN, TX 77043 PEANUT BUTTER creamy NET WT 0.75 OZ (21g) FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE WYOMING, MI 49509; CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328

Ventura Foods LLC
FDA FoodClass II

CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET WT 0.75OZ DIST BY: DYMA BRANDS, INC. ATLANTA, GA 30328; Product also sold under the following brand names: FLAVOR Fresh PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY: DYMA BRANDS, INC. ATLANTA, GA 30328; HOUSE RECIPE CREAMY PEANUT BUTTER NET WT 0.75 OZ (21.2g) DISTRIBUTED BY SYSCO COROPRATION, HOUSTON, TEXAS 77077; Katy's Kitchen SMOOTH PEANUT BUTTER NET WT 0.75 OZ (21g) MARKETED BY INDEPENDENT MARKETING ALLIANCE HOUSTIN, TX 77043 PEANUT BUTTER creamy NET WT 0.75 OZ (21g) FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE WYOMING, MI 49509; CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328

Foreign material. During production, the firm found pieces of blue plastic in a filter.

Feb 18, 2026Ventura Foods LLC
PharmaceuticalUSFDA Drugs

Testosterone 75mg, Anastrozole 4mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4079-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

Testosterone 75mg, Anastrozole 4mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4079-32.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
Medical DeviceUSFDA Devices

Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

Feb 18, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceUSFDA Devices

Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD
FDA DevicesClass III

Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor

Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.

Feb 18, 2026SUREPULSE MEDICAL LTD
PharmaceuticalUSFDA Drugs

ESTRADIOL, 20 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3020-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

ESTRADIOL, 20 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3020-32.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)

Install The Recall File App

Check safety warnings, scan your pantry, and monitor your vehicles directly from your home screen.