Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,151–2,200 of 15,186
- Class II
Medical Device Recall · February 3, 2026
Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05Impactor handle may be missing cross-pin
- Class III
Drug Recall · February 3, 2026
Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Annora Pharma Pvt. LTd., Sengareddy - 502313, Telengana, IndiPresence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg
- Class II
Food Recall · February 3, 2026
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not solLabel declares bovine colostrum but does not declare milk allergen.
- Class II
Food Recall · February 3, 2026
Cocos Wholesale and Imports, LLC
Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, Net Wt. 8 oz. (227g), Keep Frozen, packaged in a plastic container, UPC 0680334992716Label lists flour as a sub-ingredient of the shells, and ricotta cheese as a sub-ingredient of the cream but does not declare wheat or milk.
- Class II
Medical Device Recall · February 3, 2026
Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LPThere is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.
- Class II
Medical Device Recall · February 3, 2026
IBA Proton Therapy System - PROTEUS 235It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS does not interrupt the beam delivery if the Healthy Signal from an external gating device is lost. This may lead to a risk of mistreatment when external gating devices are used.
- Unclassified
Vehicle Recall · February 2, 2026
2024 JEEP WAGONEER S, 2025 JEEP WAGONEER S, 2025 RAM 5500, 2025 RAM 3500, 2026 JEEP CHEROKEE, 2026 RAM 3500Trailer brake lights and turn signals that do not illuminate reduce visibility to other drivers, increasing the risk of a crash. Additionally, trailer brakes that fail increase the risk of a crash.
- Class II
Medical Device Recall · February 2, 2026
Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be usThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
- Class II
Drug Recall · February 2, 2026
Pro Numb Tattoo Numbing Spray LLC
Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11cGMP deviations
- Class II
Medical Device Recall · February 2, 2026
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
- Class II
Medical Device Recall · February 2, 2026
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intenThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
- Class II
Medical Device Recall · February 2, 2026
Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation andThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
- Unclassified
Vehicle Recall · February 1, 2026
2025 VOLVO EX30A high-voltage battery that overheats increases the risk of a fire.
- Class II
Medical Device Recall · February 1, 2026
On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
- Class I
Food Recall · January 31, 2026
Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK,Undeclared hazelnut.
- Class I
Food Recall · January 30, 2026
Karns Foods, Mini Dark Chocolate Raspberry Cups, 8 oz Clear plastic tamper evident packs, 36-42 packed per breakoutProduct may contain undeclared peanuts.
- Class II
Medical Device Recall · January 30, 2026
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15 minutes may lead to: Reagent Blank and calibration databases not opening errors: CAL History DB Open Error.., RB History DB Open Error..; system will stop analyzing, firm service must visit to apply software solution; may lead to delay in diagnosis and/or patient treatment
- Class II
Medical Device Recall · January 30, 2026
Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-02There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- Class I
- Class II
Food Recall · January 30, 2026
Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label iIngredients List declares peanut but the Contains statement does not declare peanut
- Class II
Medical Device Recall · January 30, 2026
MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and 6.62), which could result in a risk of hypoglycemia or hyperglycemia due to inaccuracies in insulin delivery (either under-delivery, over-delivery, or cessation of delivery).
- Class I
Food Recall · January 30, 2026
The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 789953, NET WT. 5 LB (2.26 kg) per plastic tub. UPC 7 5810830149 8. Distributed byUndeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.
- Class II
Medical Device Recall · January 30, 2026
Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Number: DYNJ908126; 3) CARDIO CONGENITO, Model NumbeThe instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.
- Class II
Medical Device Recall · January 30, 2026
DxC 700 AU, REF: B86444, B86446A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15 minutes may lead to: Reagent Blank and calibration databases not opening errors: CAL History DB Open Error.., RB History DB Open Error..; system will stop analyzing, firm service must visit to apply software solution; may lead to delay in diagnosis and/or patient treatment.
- Class II
Medical Device Recall · January 30, 2026
Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- Class II
Medical Device Recall · January 30, 2026
Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge,The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the infusion set is connected to the body, when it should instead direct users to confirm that the infusion set is not connected to the body. Following this instruction could result in unintended insulin delivery, potentially leading to a hypoglycemic event.
- Class II
Medical Device Recall · January 30, 2026
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 1Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient monitoring system.
- Class II
Medical Device Recall · January 30, 2026
Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 58There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- Class II
Medical Device Recall · January 29, 2026
Olympus Corporation of the Americas
Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent lPotential for rubber fragment detachment during use.
- Unclassified
Consumer Product Recall · January 29, 2026
Arizona Nutritional Supplements, of Chandler, Arizona
Ultimate Multivitamin+ Dietary Supplement BottlesThe bottles are filled with dietary supplements containing iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.
- Unclassified
Consumer Product Recall · January 29, 2026
Gazelle USA, LLC, of Santa Cruz, California
Urban Arrow FamilyNext Pro Cargo E-BikesThe buckle can fail to fully latch when used with children in the cargo area, posing injury hazards to children.
- Unclassified
Consumer Product Recall · January 29, 2026
Hobby Lobby Stores, Inc. of Oklahoma City, Oklahoma
Giraffe Plush Toy with clip, Llama Plush Toy with clipThe legs of the plush toy can detach from the body allowing the release of small beads that are on the legs, posing a choking hazard to young children.
- Unclassified
Consumer Product Recall · January 29, 2026
Rear wheel bolts installed on model year 2026 Trek FX+ 1 and Electra Townie Go! electric bicyclesThe rear wheel bolts can break when torqued, causing the wheel to separate from the bicycle, posing a fall hazard.
- Unclassified
Consumer Product Recall · January 29, 2026
Starmatrix Group Inc., of China
Sunneday and Blue Bay brand 48-inch and taller above-ground poolsThe compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk.
- Unclassified
Consumer Product Recall · January 29, 2026
Primark US Corp. of Boston, Massachusetts
Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring SetThe crayons in the coloring set have high levels of strontium and aluminum, and this may present a risk if ingested, posing a poisoning hazard if ingested by young children.
- Class II
Food Recall · January 29, 2026
a.) Preema brand Bright Red Food Colour Powder; Net Weight .88oz/25gm; packaged in small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT,Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Software Version: N/A Product Description: CESK SHANDS JACKSONVILLE 20055717 ComponeB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: NoB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP CATH Model/Catalog Number: 530201 Software Version: N/A Product Description: NES1725KFXL SPINAL EPID CLOSED TIP CB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM Model/Catalog Number: 552126 Software Version: N/A Product Description: CESK RIVERSIDE HEALTH SYSTEM Component: NoB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description: CESK HARRIS METHODIST Component: NoB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Class II
Medical Device Recall · January 29, 2026
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervationDue to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
- Class II
Medical Device Recall · January 29, 2026
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervationDue to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
- Class II
Drug Recall · January 29, 2026
Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963-678-11Failed Dissolution Specifications
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK, BLOCKJOCKS TRAY Model/Catalog Number: 570246 Software Version: N/A Product Description: BPSK, BLOCKJOCKS TRAY Component: NoB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Unclassified
Consumer Product Recall · January 29, 2026
Shenzhen Mailesi Technology Co., Ltd., dba Vanfun, of China
AiTuiTui Pull String Teething ToysThe hair growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum bottle is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model/Catalog Number: 530134 Software Version: N/A Product Description: SESK UPMC DOUBLE CATHETER TRAY Component: NoB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
- Class II
Medical Device Recall · January 29, 2026
Olympus Corporation of the Americas
Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent refPotential for rubber fragment detachment during use.