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

2751–2775 of 113817

HighFDA (Devices)·Z-1857-2026·2026-04-29
Soft-Vu Angiographic Catheter Kumpe Non-Braided manufacturing defect recall
Angiodynamics is recalling Soft-Vu Angiographic Catheter Kumpe units due to a manufacturing defect that may prevent guidewires from passing through the catheter hub.
Product
Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.: 10710013; Product/UPN No.: H787107100135 (Box), H787107100130 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2026·2026-04-29
AccuVu Angiographic Catheter Manufacturing Defect Recall Worldwide
Angiodynamics is recalling AccuVu Angiographic Catheters worldwide due to a manufacturing defect that may prevent guidewires from passing through the catheter hub's inner diameter.
Product
AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM; Catalog No.: 13709604; Product/UPN No.: H787137096045 (Box), H787137096040 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0672-2026·2026-04-29
Bulk horchata powder recalled nationwide over undeclared milk
Bulk Horchata Powder is being recalled because of undeclared milk. The action covers 2,494 cases of 25 lbs each, distributed across a large number of states.
Product
Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547
Category
Food
Distribution
29 states
HighNHTSA·26V272000·2026-04-29
Newmar Recalls 2026 Freedom Aire Motorhomes Due to Spoiler Detachment Risk
Newmar is recalling 2026 Freedom Aire motorhomes because the front chin spoiler may detach during transit, creating a road hazard.
Product
NEWMAR — NEWMAR FREEDOM AIRE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2026·2026-04-29
Olympus Thunderbeat II Shears Ultrasonic Mode distal tip detachment risk
Olympus is recalling Thunderbeat II Shears (5mm, 45cm) because the distal tip component may detach during use, potentially causing patient harm.
Product
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1856-2026·2026-04-29
Soft-Vu Angiographic Catheter Pigtail Non-Braided Guidewire Passage Defect
Angiodynamics is recalling Soft-Vu Angiographic Catheter (Pigtail, Non-Braided) due to a manufacturing defect that may prevent a guidewire from passing through the catheter hub's inner diameter.
Product
Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No.: 10707103; Product/UPN No.: H787107071035 (Box), H787107071030 (Pouch); Box Quantity: 10;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1916-2026·2026-04-29
MAC two-lumen central venous kits recalled over incorrectly manufactured adhesive
The MAC Two-Lumen Central Venous Access Kit is being recalled after a supplier notified the firm that the liquid adhesive used in the device was incorrectly manufactured.
Product
MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous Access Device permits short-term (<30 days) venous access and catheter introduction
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1923-2026·2026-04-29
Oxoid Agglutinating Sera Salmonella 9-0 Serotyping Classification Error
Remel Europe Ltd. is recalling specific lots of Oxoid Agglutinating Sera, Salmonella 9-0 due to cross-reactivity that may misidentify Salmonella 9-O serotypes as 2-O serotypes in laboratory testing.
Product
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1939-2026·2026-04-29
Diversatek Healthcare Viper Balloon Dilator catheter inflation tag error
Diversatek Healthcare is recalling Viper 3-Stage Wire Guided Balloon Dilators because the catheter inflation tag may contain an incorrect part number with wrong balloon diameter sizes and inflation pressures.
Product
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 12mm-13.5mm-15mm, REF 1205-15
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-1863-2026·2026-04-29
Soft-Vu Angiographic Catheter Berenstein Non-Braided Device Recall
Angiodynamics is recalling Soft-Vu Angiographic Catheters (Berenstein, Non-Braided) due to a manufacturing defect that may prevent the guidewire from passing through the catheter hub. The defect affects 1,030 units distributed worldwide.
Product
Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog No.: 10714016; Product/UPN No.: H787107140165 (Box), H787107140160 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1927-2026·2026-04-29
Sequencing Agent SEQ0067 Component Recalled for Potential False-Positive Results
Foundation Medicine is recalling Sequencing Agent SEQ0067, a component of the FoundationOne CDx test, due to a possible increase in phasing that could result in false-positive BARD1 splice site indel artifact variants.
Product
Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1894-2026·2026-04-29
LeadCare Plus Blood Lead Test Kit Recalled for Unexpectedly Elevated Results
Magellan Diagnostics is recalling LeadCare Plus Blood Lead Test Kits (Catalog Number 82-0004) because they may produce falsely elevated lead results when used with certain third-party micro-collection devices, potentially causing delayed testing and unnecessary follow-up testing.
Product
LeadCare¿ Plus Blood Lead Test Kit; Catalog Number: 82-0004; The LeadCare¿ Plus kit is provided with the following materials: " Sensors (4 containers of 24 each; 96 tests) " Treatment Reagent Tubes (4 packages of 24 each; 96 tests) " Calibration Button (1 @) " Lead Contro
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1930-2026·2026-04-29
Foley Urine Collection Kit recalled for non-sterile alcohol prep pads
LSL Healthcare is recalling its Foley Urine Collection Kit (Model 1555) because it contains Webcol Large Alcohol Prep Pads that are non-sterile. The kits were distributed nationwide in Maryland, Illinois, and Minnesota.
Product
LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V273000·2026-04-29
Newmar Recalls 2026 Freedom Aire Motorhomes for Incorrect Weight Labels
Newmar is recalling 2026 Freedom Aire motorhomes because the Cargo Carrying Capacity label may display an incorrect weight value, potentially allowing the vehicle to be overloaded.
Product
NEWMAR — NEWMAR FREEDOM AIRE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1922-2026·2026-04-29
Beckman Coulter Access Total T4 Calibrator Recalled for Inaccurate Results
Beckman Coulter is recalling Access Total T4 Calibrator lots because they produce falsely low patient results on DxI 600/800 instruments, potentially leading to unnecessary testing, delayed treatment for thyroid disorders, and incorrect dosing in pregnant patients.
Product
Access Total T4 Calibrator, Catalog No. 33805
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1851-2026·2026-04-29
Olympus Thunderbeat II Shears recall due to distal tip detachment
Olympus Corporation of the Americas is recalling Olympus Thunderbeat II Shears (Model TB2-0520FC) because the distal tip component may detach during use.
Product
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1920-2026·2026-04-29
IV Administration Sets from Windstone Medical for Infusion Pump Systems
Windstone Medical Packaging is recalling Custom Convenience Kits Pre Op Kit units due to potential backflow of medication between IV containers and risk of priming failure in gravity and pump administration sets.
Product
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1872-2026·2026-04-29
AccuVu Angiographic Catheter recall due to manufacturing defect
Angiodynamics is recalling AccuVu Angiographic Catheters due to a manufacturing defect that may prevent a guidewire from passing through the catheter hub. The defect could interfere with proper device function during medical procedures.
Product
AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; Catalog No.: 13709005; Product/UPN No.: H787137090055 (Box), H787137090050 (Pouch); Box Quantity: 5 pouches;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1808-2026·2026-04-29
Handheld UV-C germicidal wand recalls for excessive radiation exposure
Uvlizer handheld UV-C germicidal wands may expose users and nearby people to ultraviolet radiation at levels above international safety guidelines for skin and eye protection.
Product
The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x 3. The product has two peak emission wavelengths at 274 nm and 397 nm.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1896-2026·2026-04-29
Avitene Ultrafoam Microfibrillar Collagen Hemostat Recalled for Foreign Matter
Davol, Inc. is recalling Avitene Ultrafoam Microfibrillar Collagen Hemostat (Catalog Number 1050030) because the product may contain foreign matter, confirmed to be inspect fragments.
Product
Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1807-2026·2026-04-29
Ultraviolet-C Germicidal Wand Recalled for Unsafe UVC Radiation Exposure
Uvlizer handheld UV-C wands may expose users and bystanders to ultraviolet-C radiation levels above international safety limits during normal use, posing risk of skin and eye injury.
Product
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1912-2026·2026-04-29
Arrow Percutaneous Sheath Introducer Catheter Recall Due to Adhesive Defect
Arrow International is recalling 115 units of its percutaneous sheath introducer with 7.5–8 Fr catheter because the liquid adhesive was incorrectly manufactured by a supplier. The product is used for venous access and central circulation catheterization.
Product
PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1904-2026·2026-04-29
Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes Recall
Olympus Corporation of the Americas is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2116) because the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Product
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V271000·2026-04-29
Roadtrek recreational vehicle pop-top latches may disengage during transit
Roadtrek is recalling certain recreational vehicles because the pop-top latch may disengage during transit, causing the pop-top to lift. 312 vehicles are affected.
Product
ROADTREK — ROADTREK PLAY SLUMBER, PIVOT SLUMBER, PLAY TUFF SL, PLAY+SLUMBER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0671-2026·2026-04-29
Spice powder recalled after lead level exceeded the New York standard
A 4 oz spice powder is being recalled because its lead level was higher than the New York State Department of Agriculture and Markets standard. 20 cases are affected.
Product
Spice Powder, 4 oz, Plastic Bag
Category
Food
Distribution
8 states

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2751–2775 of 113817