Safety Recalls
RSS ↗17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,701–3,750 of 17,559
- Class I
- Class II
Drug Recall · January 29, 2026
Metoprolol Succinate Extended-Release Tablets, 25 mg, 100 tablets bottles (NDC: 45963-709-11) and 1,000 tablets bottles (NDC: 45963-709-96), Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054Failed Dissolution Specifications
- 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.
- 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.
- Unclassified
Vehicle Recall · January 29, 2026
Honda (American Honda Motor Co.)
2023 HONDA ACCORD HYBRID, 2024 ACURA INTEGRA, 2024 HONDA HR-V, 2024 HONDA PILOTA loose driver's seat may not adequately restrain the driver during a crash, increasing the risk of injury.
- Unclassified
Vehicle Recall · January 29, 2026
2023 JEEP GRAND CHEROKEE L, 2023 JEEP GRAND CHEROKEERear coil springs that detach from the vehicle while driving increase the risk of a crash.
- 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
Drug Recall · January 29, 2026
Metoprolol Succinate Extended-Release Tablets, 50 mg, 100 tablets bottles (NDC: 45963-676-11) and 1,000 tablets bottles (NDC: 45963-676-96), Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054Failed Dissolution Specifications
- Class II
Medical Device Recall · January 29, 2026
Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID Model/Catalog Number: 530184 Software Version: N/A Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPIDB. 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.
- Unclassified
Consumer Product Recall · January 29, 2026
Ganzhounengmiaokejiyouxiangongsi dba Nengmiaokeji, of China
Sefudun Hair Growth Serum KitsThe 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
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.
- 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.
- Unclassified
Consumer Product Recall · January 29, 2026
Shenzhen Shimei Lighting Co., Ltd dba as Luxjet, of China
LuxJet Submersible LED LightsThe recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- Unclassified
Consumer Product Recall · January 29, 2026
Northern Tool + Equipment Manufacturing, of Faribault, Minnesota
NorthStar Hot Water Pressure WashersThe fan wheel on the recalled pressure washers can fail, causing abnormal burner operation that can produce smoke and/or bursts of flames during use, posing a fire hazard.
- 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
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.
- Class II
Drug Recall · January 29, 2026
Metoprolol Succinate Extended-Release Tablets, Rx Only, 100 mg, 100 tablets bottles (NDC: 45963-677-11) and 1,000 tablets bottles (NDC: 45963-677-96), Teva Pharmaceuticals, Parsippany, NJ 07054.Failed Dissolution Specifications
- 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: 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
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 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: 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: 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.
- 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.
- 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.
- 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
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.
- Unclassified
Consumer Product Recall · January 29, 2026
Bangkit USA Inc, dba Bazic Products, of El Monte, California
Bazic Silicone GlueThe glue contains methanol, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The glue's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children. In addition, the glue violates the labeling requirements under the Federal Hazardous Substances Act because it is incorrectly labeled as "Non-Toxic" and because it lacks a "highly flammable" hazard statement.
- Unclassified
Consumer Product Recall · January 29, 2026
Guangzhou Runshu BioTech Co., Ltd. of China
Viofairy Hair Growth SerumThe serum bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.
- 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 28, 2026
Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
- Class I
Food Recall · January 28, 2026
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING
Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 810093891320Undeclared allergen ingredient (Wheat and Sesame)
- Class I
Food Recall · January 28, 2026
Art Monkey LLC dba Why Not Natural
Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.Potential to be contaminated with Salmonella
- Class I
- Class I
Food Recall · January 28, 2026
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING
Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 810093891325Undeclared allergen ingredient (Wheat and Sesame)
- Class II
Medical Device Recall · January 28, 2026
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXCFabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.
- Class II
Medical Device Recall · January 28, 2026
Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN DBD-DRAPE,UNDERBUTTOCK,28 X 50.5,XALT GR MDTMAYOXGNFabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.
- Unclassified
Vehicle Recall · January 28, 2026
Toyota Motor Engineering & Manufacturing
2023 TOYOTA PRIUS, 2023 TOYOTA PRIUS PRIME, 2024 TOYOTA PRIUS, 2024 TOYOTA PRIUS PRIME, 2025 TOYOTA PRIUSA door that unexpectedly opens while the vehicle is moving increases the risk of injury.
- Unclassified
Vehicle Recall · January 28, 2026
2025 DUCATI PANIGALE V4 S, 2025 DUCATI PANIGALE V4A sudden loss of rear brake function increases the risk of a crash or injury.
- Class I
Food Recall · January 28, 2026
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING
Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 810093891338Undeclared allergen ingredient (Wheat and Sesame)
- Class II
Medical Device Recall · January 27, 2026
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
- Class I
Medical Device Recall · January 27, 2026
Impella RP with SmartAssist. Product Code: 0046-0035.Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
- Unclassified
Vehicle Recall · January 27, 2026
2025 HYUNDAI TUCSON HYBRID, 2025 HYUNDAI TUCSON PLUG-IN HYBRIDAn instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.
- Class II
Medical Device Recall · January 27, 2026
CLARITY II Laser System; Model No. 1110200210.Reports of devices sparking/popping and potentially burning patients.
- Unclassified
Vehicle Recall · January 27, 2026
2025 KIA SORENTO HYBRID, 2025 KIA K4, 2025 KIA SORENTOAn instrument panel display that fails to show critical safety information, such as the speedometer, tire pressure, or warning lights, increases the risk of a crash.
- Class II
Food Recall · January 27, 2026
Product is Frozen Half Shell Oysters in 15-16 pound blocks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA SidImported oysters potentially contaminated with Norovirus
- Class II
Drug Recall · January 27, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Diclofenac Sodium, Topical Gel, 3%, 100 g tube, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 516Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
- Class I
Medical Device Recall · January 27, 2026
Impella RP Flex with SmartAssist. Product Code: 1000323.Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.