Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent Product Recall Alerts List
Showing 4,226 - 4,250 of 4,622 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
EnHomee 10-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
This recall involves EnHomee 10-Drawer Dressers. The recalled dressers were sold in the following colors: black, white, grey, and brown. They have a metal frame, wooden top, 10 collapsable fabric drawers, and two metal drawers. The dressers are 38 inches long by 11.8 inches wide by 48.1 inches tall. Model number "55SCWMSCXLBR" can be found on the order information within your Amazon account.
|
CPSC
10606
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Dresbe LED Christmas Headbands Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
This recall involves Dresbe LED Christmas Headbands. The headbands were sold as a two-pack of novelty headbands, one red headband with candy cane attachments and a green headband with a Christmas tree attachment, each containing three button cell batteries to power LED lights. The headbands have "HB-052" and "DRESBE LED Christmas Headband (2pc)" printed on labels located on the package.
|
CPSC
10600
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Cobelae Busy Books Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates Small Parts Ban; Sold on Amazon by Flyindream
This recall involves Cobelae Busy Book, model: 2025-Q3-0702. The Busy Book has a yellow and brown giraffe on the front cover. The apple on page eight of the books includes a string of beads. There are no markings on the book.
|
CPSC
10605
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
Andy & Evan Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
This recall involves Andy & Evan-branded children's pajama sets. The recalled woven pajamas consist of a long-sleeved shirt with buttons, a front pocket and matching flared pants. The pajamas were sold in pink with white stripes and purple and pink hearts with trim in children's sizes 2T, 3T, 4T, 5, 6 and 6X. "Andy & Evan" and the size are printed on the sewn-in neck label. "RN# 136762" and "YC05" are printed on the sewn-in side seam label.
|
CPSC
10607
|
Child/Baby | High |
Feb 6, 2026
Recall: Feb 5, 2026
|
Details |
|
BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System with Guardrails" Suite MX is a modular infusion pump and monitoring system for the continuous or intermittent administration of fluids to adult, pediatric, and neonatal patients through clinically accepted routes of administration: intravenous (IV), intra-arterial (IA), subcutaneous, epidural, or irrigation of fluid spaces. The BD AlarisTM System includes the PC Unit (PCU) and one or more of the following: Pump Module, Syringe Module, end-tidal CO2 (EtCO2) Module, Auto-ID Module, patient-controlled analgesia (
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only affects the Interoperability workflow for devices with a DST invalid timestamp, impacting connectivity of the PCU to the hospital network
|
FDA
Z-1217-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Nov 6, 2025
|
Details |
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Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK, Kit SKU DYNJ16826O
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.
|
FDA
Z-1198-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
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Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy, Elekta Harmony, Elekta Infinity, Versa HD Software Version: N/A Product Description: Digital Linear Accelerator Component: No
Due to a manufacturing issue and electrical grounding of systems.
|
FDA
Z-1164-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 14, 2025
|
Details |
|
Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity Standard Solutions are a secondary standard solution used for the calibration of conductivity cells together with conductivity meters
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.
|
FDA
Z-1185-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
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Alphenix INFX-8000C, interventional fluoroscopic x-ray system
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
|
FDA
Z-1176-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 19, 2025
|
Details |
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Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS, Kit SKU CDS984347O; 2) HEAD AND NECK CDS-LF, Kit SKU CDS984857N; 3) NECK PACK-LF, Kit SKU DYNJ0966130K; 4) NECKLINE PACK-LF, Kit SKU DYNJ51440B; 5) THYROID PACK, Kit SKU DYNJ58742J; 6) ENT I, Kit SKU DYNJ63781B; 7) NECK PACK, Kit SKU DYNJ82751B; 8) NOSE PACK, Kit SKU DYNJ82753C; 9) WMC COCHLEAR IMPLANT ADD ON, Kit SKU DYNJ907206G.
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.
|
FDA
Z-1190-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
|
Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Potential exposure of rodents and rodent activity in the distribution center.
|
FDA
Z-1180-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 26, 2025
|
Details |
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Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, Kit SKU DYNJ0660040R; 2) PLASTICS VCH, Kit SKU DYNJ39225K; 3) WT BREAST PACK, Kit SKU DYNJ46620I; 4) ENDO / AUG PACK, Kit SKU DYNJ59250I; 5) KMC PLASTIC/GEN PACK-LF, Kit SKU DYNJ65980J; 6) PLASTICS PACK, Kit SKU DYNJ68288A; 7) IMPLANT REMOVAL KIT, Kit SKU MNS13035; 8) PLASTICS PACK-LF, Kit SKU PHS41746D.
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.
|
FDA
Z-1192-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
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Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
|
FDA
Z-1114-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 15, 2025
|
Details |
|
Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version R11.1 and R12.1.
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
|
FDA
Z-1206-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 3, 2025
|
Details |
|
Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMAKER/ICD PACK, Kit SKU DYNJ33822L; 3) VENOUS ACCESS PACK, Kit SKU DYNJ45640B; 4) PACEMAKER SET UP, Kit SKU DYNJ63377D; 5) PACK PACEMAKER CUSTOM,9909178, Kit SKU DYNJ65011D; 6) HEART BASIC OPEN PACK, Kit SKU DYNJ69143C; 7) SCC VEIN PACK, Kit SKU DYNJ69313; 8) CV PACK, Kit SKU DYNJ86007B.
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.
|
FDA
Z-1188-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 12, 2025
|
Details |
|
Genesis Screw-In Anchor
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
|
FDA
Z-1168-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 17, 2025
|
Details |
|
Alphenix INFX-8000V, interventional fluoroscopic x-ray system
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
|
FDA
Z-1179-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 19, 2025
|
Details |
|
PREGNANCY TEST 24CT
Potential exposure of rodents and rodent activity in the distribution center.
|
FDA
Z-1184-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 26, 2025
|
Details |
|
Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Version VB10D-SP02
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.
|
FDA
Z-1175-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 29, 2025
|
Details |
|
Alphenix INFX-8000H, interventional fluoroscopic x-ray system
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
|
FDA
Z-1178-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 19, 2025
|
Details |
|
Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: no
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
|
FDA
Z-1117-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 15, 2025
|
Details |
|
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Incorrect expiration date
|
FDA
Z-1218-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 5, 2025
|
Details |
|
Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, TROJAN CONDOMS MAGNUM 48 CT DISP, *BOX TROJAN CONDOMS MAGNUM 50CT .
Potential exposure of rodents and rodent activity in the distribution center.
|
FDA
Z-1181-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 26, 2025
|
Details |
|
Genesis Dual Thread Screw-In Anchor
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
|
FDA
Z-1169-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 17, 2025
|
Details |
|
Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer Model/Catalog Number: 7730ALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
|
FDA
Z-1116-2026
|
Medical Device | High |
Feb 4, 2026
Recall: Dec 15, 2025
|
Details |
Recent Product Recall Alerts
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-Risk Recall Updates
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
Daily Official Source Coverage
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
Latest Recalls By Source Agency
Use the source notes to understand which agency published the notice and what type of product it covers.
Latest Consumer Product Recalls
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Latest Food And Medical Device Recalls
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
Latest Meat And Poultry Recall Alerts
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
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New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
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Check The Publish Date First
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Prioritize High-Risk Notices
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Verify The Official Notice
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
Latest Product Recalls FAQ
Helpful context for searches such as product recalls today, recent product recalls and recall alerts.
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The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
Why do some recent recalls have older recall dates?
Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.
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Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
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