Product Recall Checker | Search Product Recalls by UPC, Lot Code, Brand or Model

Latest Product Recall Matches

Showing 2,876 - 2,900 of 3,318 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
GM Gumili Wintergreen Essential Oil Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Gumili Beauty This recall involves GM Gumili Wintergreen Essential Oil. The essential oil was sold in an amber glass bottle with a black screw-on cap and a white label with the "GM" logo, "gumili," "wintergreen essential oil" and an image of a wintergreen plant. The packaging box is white with blue text with the "GM" logo, "gumili," "essential oil" and "100% pure & natural" on the front. The back of the box has directions, safety instructions and the manufacturer's information. A black dropper cap was included with the oil.	CPSC 10596	Child/Baby	High	Feb 6, 2026 Recall: Feb 5, 2026	Details
Furnulem 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units This recall involves Furnulem five-drawer dressers. The wooden, white dressers measure about 31.5 inches tall, 15.75 inches long and 50.2 inches wide. They have a top with recessed power outlets, and each drawer has two round pull knobs. Only dressers that did not come with feet extensions are included in this recall. Model "HK-DS-017-CL-5D-1-W" is printed on the packaging.	CPSC 10598	Child/Baby	High	Feb 6, 2026 Recall: Feb 5, 2026	Details
Fixwal 7-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 the Fixwal 7-Drawer Dressers. The recalled dressers were sold in black and white and have a metal frame, wooden top, and seven collapsable fabric drawers. The dressers are 55.1 inches long by 11.8 inches wide by 31.5 inches tall.	CPSC 10599	Child/Baby	High	Feb 6, 2026 Recall: Feb 5, 2026	Details
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
Clark Associates Recalls Lancaster Table & Seating Powder-Coated Aluminum Outdoor Restaurant Chairs and Barstools Due to Fall Hazard This recall involves three models of Lancaster Table & Seating Powder-Coated Aluminum Outdoor Chairs and Barstools in arm chair, side chair (no arms) and barstool configurations sold under 180 item numbers. The chairs and barstools were sold in blue, brown, dark gray, light gray/silver, red, white, aqua, black, green, sangria/burgundy, yellow and orange. The chairs were sold with and without accompanying outdoor tables, which are not subject to the recall. The item numbers can be found on order confirmation emails, shipping confirmation emails and invoices. A full list of affected item numbers and examples of colors are available at www.webstaurantstore.com/uploads/Clark_Associates/2026/1/lts-recall-list-of-affected-products-1.pdf.	CPSC 10604	Household	Unknown	Feb 6, 2026 Recall: Feb 5, 2026	Details
Aterian Recalls PurSteam Elite Travel Steamers and Mighty Lil Steamers Due to Risk of Serious Burn Injury This recall involves PurSteam Elite Travel Steamers and PurSteam Mighty Lil Steamers purchased after December 2020 or with one of the following date codes: 2310, 2308, 2305, 2304, 2303, 2212, 2211, 2210, 2203, 2112, 2111, 2110, 0221, 1019, and 4619. The PurSteam Elite Travel Steamer is white with a triangular-shaped opening for the steam vents. The "PurSteam" logo is printed below a wave-shaped water reservoir window, and "Model: PS-510" is printed on a label on the bottom of the product. The PurSteam Mighty Lil Steamer is white with an oblong-shaped opening for the steam vents. The "PurSteam" logo is printed below the water reservoir window, and "Model: PS 550" is printed on a label on the bottom of the product. On both steamer models, the manufacture date (date code) is located on a label on the bottom of the product in YYMM format.	CPSC 10601	Consumer Product	Medium	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
Park Outside - High Voltage Battery May Overheat Jaguar Land Rover North America, LLC (Jaguar) is recalling certain 2020-2021 Jaguar I-PACE vehicles. The high voltage battery may overheat. A high voltage battery that overheats increases the risk of a fire.	NHTSA 26V067000	Vehicle	Unknown	Feb 5, 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
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
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
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
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
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
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

Showing 2,876 - 2,900 of 3,318 product recalls

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A recall usually applies to specific products, batches, model ranges or dates. Use the details printed on the item, package, label, receipt or vehicle paperwork.

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This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.

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How To Confirm A Recall Match

1. Search The Obvious Name First

Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.

2. Open The Closest Result

Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.

3. Match Every Identifier

Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.

4. Follow The Official Remedy

The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.

When A Recall Result Looks Like Your Product

Use this checklist before you throw away a product, call the company, request a refund or schedule a repair.

If It Is Food, Formula Or Pet Food

Do not rely on brand alone. Match the package size, UPC, lot code, best-by date, use-by date, distribution states and any allergy or contamination warning.

If It Is A Baby Or Household Product

Look for model number, date code, serial range, color, size, online listing, product photo and the exact hazard such as choking, suffocation, fire or fall risk.

If It Is A Vehicle Or Car Seat

Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.

If The Details Do Not Match

Your item may not be part of that specific recall. Check spelling, older notices, retailer alerts and the official source before deciding it is safe.

What Is A Product Recall?

A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.

What Should You Do After Finding A Recall?

If all affected details match, follow the official instructions. Keep packaging, take photos, save receipts and contact the company or retailer when a refund or repair is offered.

Why Recall Details Must Match Exactly

A similar brand or product name is not enough. UPCs, lot codes, dates, model numbers, serial ranges and distribution areas determine whether your item is included.

How To Avoid Fake Recall Notices

Be careful with text messages, social posts or refund forms that ask for private information. Verify the notice through an official agency, retailer or manufacturer page.

Product Recall FAQ

Short answers for common product recall searches.

Can I search product recalls by UPC code?

Yes, when the official recall notice includes a UPC or product code. If no result appears, also search the brand, product name, package size, lot code and company name.

Can I search product recalls by lot code?

Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.

Does this replace a VIN recall lookup?

No. This tool helps find vehicle recall campaigns and NHTSA numbers. Use the official NHTSA VIN or license plate lookup for vehicle-specific unrepaired recall status.

Are all recalls listed here?

The database combines multiple official U.S. sources, but agencies and companies can publish or update notices at different times. Always check the linked official notice before taking final action.

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