Home / Recalls
Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
March 26, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape.
Hazard: Potential breach in pouch packaging which could lead to loss of sterility.
March 26, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Proxima Drape labeled as PACK,BASIC,SIRUS,V,5/CS; PACK,BASIC IV,SIRUS,5/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,SET UP,NO D
Hazard: Potential breach in pouch packaging which could lead to loss of sterility.
March 26, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW; SHEET, DRAPE, SPLIT, ST,10/CS; DRAPE,LAPROSCOPY,CHOLE,W/TROUGH,ST,8/
Hazard: Potential breach in pouch packaging which could lead to loss of sterility.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls VEIN TRAY, Model No UTVT21C UTVT21C02 UTVT21C-03
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls THORACIC PACK , Model No UTTC82Y UTTC82AA-01
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls SPINE LUMBAR PACK , Model No UTSL72AA UTSL72AB
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls OPEN HEART A PACK , Model No UTOH19AI UTOH19AJ-01 UTOH19AJ-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls MAJOR VASCULAR PACK , Model No UTMV78X-01 UTMV78Y UTMV78Y-01 UTMV78X-01 UTMV78Y-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls GENERAL LAPAROSCOPIC PACK-LF , Model No UTGL53S-06 UTGL53S-07 UTGL53S-08
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls AV FISTULA , Model No UTAV77T
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls NEURO IR TRAY , Model No WENI56J
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls DIAGNOSTIC NEURO IR TRAY , Model No WENE21
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls CV BASIC PUMP PACK , Model No WECV23D
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LAPAROSCOPY PACK , Model No SFLA02A SFLA02B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls EAR PACK , Model No SFEA12A
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls DELIVERY PACK , Model No SGDV22D-01 SGDV22E
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls TOTAL HIP PACK , Model No SMTH06O SMTH06P
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls CYSTO , Model No SACY80R
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls URO ROBOTIC PACK , Model No LVUR44C LVUR44C-03
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LABOR & DELIVERY PPS , Model No LLLD64O LLLD64O-01 LLLD64O-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls CENTRAL LINE PICC , Model No LLCL44H LLCL44H-01
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls C-SECTION PPS , Model No LLCI66M LLCI66M-02 LLCI66M-03 LLCI66M-04
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls BORN ON ARRIVAL KIT , Model No LLBN11B
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls GENERAL ANGIO PACK , Model Nos LLAP75G LLAP75G-01 LLAP75G-02 LLAP75G-03
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls OPEN HEART ADULT - SIDE A , Model Nos LLOH01I-01 LLOH01I
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LABOR & DELIVERY PACK, Model Nos LLLD19H
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls LAPAROSCOPY PACK, Model Nos LLLA21J LLLA21J-02
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
March 26, 2025Medical DevicesFDA
American Contract Systems Inc recalls C-SECTION PACK, Model Nos LLCS44F LLCS44F-01
Hazard: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.