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Consumer Product Recalls

127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.

February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMA
Hazard: Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF, Kit SKU DYNJ64837C; 2) LOOP R
Hazard: Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713
Hazard: Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
NIPRO Technical Services, Inc. recalls Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conducti
Hazard: due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls PREGNANCY TEST 24CT
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT; ADULT TOOTHPASTE W B
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS T
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CO
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000V, interventional fluoroscopic x-ray system
Hazard: It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000H, interventional fluoroscopic x-ray system
Hazard: It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000F, interventional fluoroscopic x-ray system
Hazard: It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000C, interventional fluoroscopic x-ray system
Hazard: It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Ve
Hazard: Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
February 4, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Ve
Hazard: Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls AlternatiV+ Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls AlternatiV+ Max Knotless Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Push-In Suture Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Knotless Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Dual Thread Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Fixone Biocomposite Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Fixone Hybrid Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Cerapedics, Inc. recalls PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Hazard: Incorrect expiration date
February 4, 2026Medical DevicesFDA
Elekta, Inc. recalls Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy, Elekta Harmony, Elekta Infinity, Versa HD
Hazard: Due to a manufacturing issue and electrical grounding of systems.
February 4, 2026Medical DevicesFDA
SunMed Holdings, LLC recalls Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Versio
Hazard: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
February 4, 2026Medical DevicesFDA
SunMed Holdings, LLC recalls Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer Model/Catalog Number: 7730ALS Software Ve
Hazard: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
February 4, 2026Medical DevicesFDA
SunMed Holdings, LLC recalls Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Ve
Hazard: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
February 4, 2026Medical DevicesFDA
SunMed Holdings, LLC recalls Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software V
Hazard: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
February 4, 2026Food & BeverageFDA
Weaver's Brew LLC recalls Goldenroot Yuzu Ginger Lemongrass Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32817 7. Keep Cold. Manufactured By Golde
Hazard: Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.