Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

1176–1200 of 113805

ModerateFDA (Devices)·Z-2667-2026·2026-07-08
Provena Midline Catheters recalled due to deficient manufacturing practices
Bard Access Systems is recalling Provena Midline Catheters because lidocaine ampoules used in manufacturing were produced under deficient manufacturing practices by a supplier.
Product
CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154003 S4153108BP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741153990 S4153108D Provena Midline
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2657-2026·2026-07-08
DuoGlide Short-Term Dialysis Catheter recall due to deficient manufacturing
Bard Access Systems is recalling lidocaine ampoules used with DuoGlide Short-Term Dialysis Catheters due to deficient manufacturing practices by the supplier. The catheters are used for temporary vascular access for hemodialysis.
Product
5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 The intended use of the Short-Term Dialysis Catheter is attaining temporary/short-term (less than 30 days) vascular access for hemodialysis, hemoperfusion, or apheresis thera
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1135-2026·2026-07-08
Dietary Supplement Vista MAX Recalled for Undeclared Yellow #5 Allergen
Vista MAX dietary supplement contains undeclared Yellow #5 dye. Consumers allergic to or sensitive to Yellow #5 should not consume the product.
Product
Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201 UPC: PHF-C023
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-2547-2026·2026-07-08
Medline Ophthalmic Pack with Lidocaine Injection Kits Recalled
Medline is recalling Ophthalmic Pack convenience kits containing Huons Lidocaine HCL Injection due to quality issues identified during an FDA manufacturing inspection. The recall affects 180 kits distributed nationwide.
Product
Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO, Model Number: DYNJ57922A
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2656-2026·2026-07-08
Poly Midline Catheters recalled due to manufacturing defects
Bard Access Systems is recalling Poly Midline Catheters because lidocaine ampoules were manufactured under deficient manufacturing practices.
Product
CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 The Poly Per-Q-Cath Midline cathet
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2544-2026·2026-07-08
Medline Lumbar Puncture Kit recalled for Lidocaine quality issues
Medline Convenience Kits containing Huons Lidocaine HCL Injection USP 1% ampules are being recalled due to quality issues identified during an FDA manufacturing inspection. Affected kits have been distributed nationwide.
Product
Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE, Model Number: DYNDH1215
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2543-2026·2026-07-08
Medline Convenience Kits recalled due to Lidocaine quality issues
Medline Industries is recalling two convenience kits (Arterial Line Kit and Ultrasound Guided IV Securement Set) due to quality issues with included Lidocaine Ampules identified during an FDA inspection.
Product
Medline Convenience Kits: 1) ARTERIAL LINE KIT, Model Number: ART890B; 2) ULTRASOUND GUIDED IV SECUREMENT SET, Model Number: IVS3350
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2536-2026·2026-07-08
Medline Lidocaine HCL Injection Ampules Recalled for Quality Issues
Medline Industries is recalling convenience kits containing Huons Lidocaine HCL Injection USP 1% ampules due to quality issues identified during an FDA manufacturing inspection of the drug maker's site.
Product
Medline Convenience Kits: 1) MULTIMED, 7FR, 20CM, 3L, CVC BUNDLE, Model Number: ECVC5995; 2) TRIPLE LUMEN CENTRAL LINE BUNDLE, Model Number: ECVC2625; 3) INTROFLEX 6F, 1L, TB, US, Model Number: STCVC26US; 4) AVA HIGH FLOW, Model Number: ECVC3720; 5) CDP, MM, 3L, 7F, 16CM
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2633-2026·2026-07-08
CRE Wireguided 8-10mm 240cm Medical Device Recall Notice
Boston Scientific Corporation is recalling CRE Wireguided 8-10mm 240cm devices worldwide due to potential sterile breaches in the packaging pouches that could compromise device sterility.
Product
CRE Wireguided 8-10mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0714-2026·2026-07-08
Gemcitabine Injection Recalled Due to Temperature Storage Abuse
McKesson is recalling Gemcitabine Injection (1 g per 26.3 mL) due to temperature abuse—the product was stored at controlled room temperature instead of under refrigeration. The affected lot was distributed nationwide.
Product
GEMCITABINE — GEMCITABINE (GEMCITABINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2661-2026·2026-07-08
Power-Trialysis Slim-Cath Dialysis Catheters Recalled by Bard Access Systems
Bard Access Systems is recalling Power-Trialysis Slim-Cath short-term dialysis catheters due to lidocaine ampoules manufactured under deficient manufacturing practices. The recall affects multiple product models distributed nationwide and internationally.
Product
5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107177 5855300 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107184 5865120 Power-Trialysis Slim-Cath
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2645-2026·2026-07-08
Medela ENFit ExSet Enteral Extension Set Connector Compatibility Issue
Medela ENFit ExSet Strl 60 enteral extension sets may contain incorrect connectors that do not attach or misconnect to ENFit connections, potentially delaying delivery of nutritional fluids or medication.
Product
Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086 Software Version: N/A Product Description: Enteral Extension Set, Length 60 Orange-Striped Minibore Tubing, (Approx. Priming Vol. 2.00 mL), ENFit¿ Componen
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-2546-2026·2026-07-08
Medline Circumcision Trays recalled due to Lidocaine quality issues
Medline Industries is recalling three models of circumcision trays containing Lidocaine ampules due to quality issues identified during an FDA inspection of the drug manufacturer.
Product
Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY, Model Number: CIT6780; 2) CIRCUMCISION TRAY W/1.1CM CIRCLAMP, Model Number: CIT3225A; 3) CIRCUMCISION TRAY, Model Number: CIT6325
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2545-2026·2026-07-08
Medline L&D Continuous Epidural Tray Kits Recalled for Quality Issues
Medline Industries is recalling 432 L&D Continuous Epidural Tray kits nationwide due to quality issues identified with the included Lidocaine ampules during an FDA manufacturing inspection.
Product
Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY, Model Number: PAIN1699A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2653-2026·2026-07-08
Covidien Shiley Disposable Decannulation Plug product labeling error
Covidien LLC is recalling Shiley Disposable Decannulation Plug devices because the product labeling incorrectly indicates the product does not contain DEHP, when in fact the product contains 30 to 35% DEHP.
Product
Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the Covidien Shiley Disposable Decannulation Plug are: Product Number / UDI-DI code 4DCFN 10884522006576 4DCFS 10884522006583 4DFEN 10884522006606 6DCFN 10884
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2666-2026·2026-07-08
PowerPICC Catheters recalled for deficient manufacturing practices
Bard Access Systems, Inc. is recalling multiple PowerPICC catheter models due to lidocaine ampoules being manufactured under deficient manufacturing practices by the supplier.
Product
1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 PowerPICC SOLO Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034602 1174108D3 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1174108D4 PowerPICC Catheter 4 Fr Single-Lum
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2655-2026·2026-07-08
Thoracentesis and Paracentesis Trays Recalled for Deficient Manufacturing
Bard Access Systems, Inc. is recalling three models of thoracentesis and paracentesis trays due to lidocaine ampoules being manufactured under deficient manufacturing practices. The devices are used for fluid removal procedures and have been distributed nationwide and in Belgium.
Product
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI Code: 0110885403108365 TPT1000 THORACENTESIS/PARACENTESIS TRAY UDI-DI Code: 0110885403108488 The Acute Drainage devices are indicated for use in re
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2641-2026·2026-07-08
ARTIS icono biplane medical imaging system detector lift malfunction
Siemens is recalling 85 units of the ARTIS icono biplane (Model 11327600) due to potential loss of detector movement capability when adjusted to maximum or minimum lift height limits.
Product
ARTIS icono biplane. Model Number: 11327600.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0657-2026·2026-07-08
Synjardy XR Tablets Recalled Due to Manufacturing Deviations
Boehringer Ingelheim Pharmaceuticals is recalling one lot of Synjardy XR Tablets (empagliflozin and metformin hydrochloride extended-release tablets), 12.5/1000 mg due to manufacturing deviations involving incorrect detergent use and missing swab sampling.
Product
Synjardy XR Tablets (empagliflozin and metformin hydrochloride extended-release tablets), 12.5/1000 mg, 60 Tablets per Bottle, Rx only, Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA. NDC: 00597-0300-45
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0696-2026·2026-07-08
vite20 Antifungal Cream recalled due to stability testing deviations
Blaine Labs Inc is recalling vite20 Antifungal Cream (10% Undecylenic Acid) because the manufacturer discontinued required stability testing for products still on the market within expiration dates.
Product
vite20 Antifungal Cream, (10% Undecylenic Acid), 0.54 OZ (15 g) bottle, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, UPC 6 16728 00039 2.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0654-2026·2026-07-08
Fexofenadine Hydrochloride Tablets 180 mg Recalled for Impurities
SUN PHARMACEUTICAL INDUSTRIES INC is recalling Fexofenadine Hydrochloride Tablets, USP 180 mg distributed nationwide because the product failed impurities and degradation specifications. The recall affects approximately 9,048 bottles distributed across the United States.
Product
Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc., New Brunswick, NJ 08901. NDC 66336-561-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V434000·2026-07-07
Braun Recalls 2026 Chevrolet Traverse Vehicles Due to Fuel Leak Risk
Braun is recalling 2026 Chevrolet Traverse vehicles because a missing braze connection on the fuel fill line may allow fuel to leak, increasing the risk of fire.
Product
BRAUN — BRAUN CHEVROLET TRAVERSE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V435000·2026-07-07
Wabash Recalls Econex Refrigerated Bodies Due to Detaching Steps
Wabash is recalling 2021-2026 Econex Refrigerated Bodies because side door stirrup steps may detach, increasing the risk of injury or a crash.
Product
WABASH — WABASH ECONEX REFRIGERATED BODY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E043000·2026-07-07
Harbor Freight Recalls Kenway LED Towing and Submersible Light Kits
Harbor Freight Tools is recalling specific Kenway LED towing and submersible light kits because they may not illuminate properly, increasing crash risk.
Product
EXTERIOR LIGHTING:TAIL LIGHTS:BULBS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V436000·2026-07-07
Subaru Ascent, Forester, and Crosstrek vehicles with incorrect weight labels
Subaru is recalling certain 2019–2026 Ascent, 2025–2026 Forester, and 2026 Crosstrek Hybrid vehicles due to incorrect Gross Axle Weight Rating labels, which may lead to vehicle overload and increased crash risk.
Product
SUBARU — SUBARU FORESTER HYBRID, CROSSTREK HYBRID, FORESTER, ASCENT
Category
Vehicle
Distribution
Distributed nationwide

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1176–1200 of 113805