April 2025 recalls

547 recalls were announced in April 2025.

What the numbers show

Critical: 1
Severe: 125
High: 277
Moderate: 138
Low: 6

Of the 547 recalls this month scored against our rubric, 0% are Critical, 23% are Severe.

Which agencies issued them

401–500 of 547

HighFDA (Devices)·Z-1484-2025·2025-04-09
GE Healthcare PACS-IW Software Security Vulnerability Affects Patient Data Access
GE Healthcare recalled Centricity PACS-IW and related medical imaging software due to a security vulnerability allowing service credentials to be identified, potentially enabling unauthorized system access and patient data manipulation.
Product
GE Healthcare Centricity PACS-IW (PACS-IW), Model Numbers: 1) 2042988-001; 2) 2049587-009; 3) 2049587-011; 4) 2049587-012; 5) 2049587-015; 6) 2049588-012 ; 7) 2052829-001.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1492-2025·2025-04-09
Terumo CDI OneView Monitor Probe May Fail to Display Oxygen Saturation Data
Terumo's CDI OneView Hematocrit/Oxygen Saturation Probe may intermittently fail to display oxygen saturation values during clinical use. When this occurs, the monitor displays dashes and triggers a yellow low-limit alarm.
Product
Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754
Category
Medical Device
Distribution
6 states
HighFDA (Food)·F-0681-2025·2025-04-09
Lean Cuisine Lemon Garlic Shrimp Stir Fry Recalled Due to Foreign Material
Nestle-USA recalls Lean Cuisine Lemon Garlic Shrimp Stir Fry (10 oz) due to potential wood-like foreign material. Approximately 7,212 cases distributed across 37 states; check Batch Number 4214595511 (Best By September 2025).
Product
Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a paperboard carton; 10 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1504-2025·2025-04-09
Respiratory Diagnostic Cartridges Recalled for Risk of False Test Results
Qiagen is recalling 445 QIAstat-Dx Respiratory Panel Plus cartridges due to faulty units that could produce false test results. Affected devices distributed to 12 US states should not be used.
Product
Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/a
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-1515-2025·2025-04-09
Ethicon PROLENE BLU Surgical Sutures Recalled for Manufacturing Defect
Ethicon is recalling specific lots of PROLENE BLU surgical sutures due to silicone curing issues during needle manufacturing.
Product
PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1510-2025·2025-04-09
Cordis Smart Control Vascular Stent Size Mismatch Recalled
Cordis recalled 20 units of its Smart Control Vascular Stent System ILIAC due to a labeling mix-up where the external label does not match the actual stent size. Wrong-sized stents could cause serious vessel complications if implanted.
Product
Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
Category
Medical Device
Distribution
5 states
HighFDA (Food)·F-0685-2025·2025-04-09
SeaBear Clam Chowder Recalled for Potential Botulinum Contamination
SeaBear Smokedhouse Alehouse Clam Chowder pouches are recalled nationwide due to potential seal failure that could allow Clostridium botulinum contamination. Consumers should not consume the product.
Product
SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0692-2025·2025-04-09
Panang Curry Tofu Vegan GF recalled for undeclared soy allergen
Seattle Homemade Thai LLC is recalling Panang Curry Tofu Vegan GF because the label declares tofu but does not declare soy as an allergen, creating risk for consumers with soy allergies.
Product
Panang Curry Tofu Vegan GF is a refrigerated and ready to eat product, packaged in plastic box, net wt. 13.5oz. UPC 88581 149928. Label declares ingredients as Tofu, Panang Curry Paste, Carrots and Peas, Coconut Milk, Kaffir Lime Leaves.
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-0306-2025·2025-04-09
Biocon Pharma atorvastatin calcium tablets recalled for failed dissolution specifications
Biocon Pharma is recalling 2,184 bottles of Atorvastatin Calcium Tablets USP 40 mg nationwide. The product failed to meet required dissolution specifications, which may affect medication absorption.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1470-2025·2025-04-09
Nasopore nasal dressing may have compromised sterile packaging
Stryker is recalling Nasopore Standard 4cm nasal dressings because the blister seals may develop bubbles, potentially compromising the sterility barrier. Affected units should not be used.
Product
Nasopore Standard 4cm fragmentable nasal dressing, Catalog Numbers 5400-010-004 and 5400-010-004ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2025·2025-04-09
Clinical Chemistry Analyzer Recalled for Software Defect in Test Result Calculation
Beckman Coulter is recalling certain DxC 500 AU Clinical Chemistry Analyzers due to a software defect that prevents calculated test results from being recalculated when constituent tests are rerun, potentially delaying patient result reporting.
Product
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2025·2025-04-09
Ethicon Surgical Sutures Recalled Due to Silicone Curing Manufacturing Defect
Ethicon Endo Surgery recalls approximately 1,080 surgical sutures due to silicone curing issues identified during manufacturing. The defect may affect suture performance during surgical use.
Product
PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1491-2025·2025-04-09
Stryker Spine Monterey AL Implant Inserter Recalled for Potential Unlock Button Separation
Stryker Spine is recalling the Monterey AL Implant Inserter (22mm, Catalog 48019140) due to potential separation of the gold unlock button from the device. The recall affects 41 units in the United States and 3 internationally.
Product
Monterey AL Implant Inserter; 22mm; Catalog 48019140.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1516-2025·2025-04-09
Surgical Suture Recall Due to Silicone Curing Defect
Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.
Product
ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1508-2025·2025-04-09
Boppli Bedside Device Kit blood pressure monitor may fail to detect pressure changes
Boppli bedside blood pressure monitors for infants may not adequately detect blood pressure changes due to vibratory noise. Affected monitors should be moved to patient's foot and ventilator lines kept away from the isolette.
Product
Boppli: Bedside Device Kit, REF: 54-0002; Sensor Band, REF: 51-0007
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1481-2025·2025-04-09
Nasopore Nasal Dressings Recalled Due to Breached Sterility Seals
Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.
Product
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1485-2025·2025-04-09
GE Healthcare Centricity Radiology RA600 and related imaging systems login vulnerability
GE Healthcare is recalling Centricity Radiology RA600 and related imaging systems due to a security vulnerability allowing service login credentials to be identified, potentially exposing patient data to unauthorized access.
Product
GE Healthcare Centricity Radiology RA600 (RA600), Model Numbers: 1) 2022296-001; 2) 2033901-001; 3) 2038437-001; 4) 2038437-011; 5) 2038437-012; 6) 2038437-013; 7) 2038437-014; 8) 2038437-0XX; 9) 2098071-004; 10) 2109571-002; 11) 2109571-006; 12) 2109571-
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0690-2025·2025-04-09
CraftMark Oatmeal Cranberry Raisin Cookie Dough Recalled for Plastic Contamination
Craftmark Bakery is recalling CraftMark Oatmeal Cranberry Raisin Cookie Dough due to potential plastic contamination. The recall affects 119 cases distributed in California, Illinois, Maryland, and Canada.
Product
5000642 CraftMark Oatmeal Cranberry Raisin Cookie Dough, 8 poly bags of 18 frozen pucks in a corrugate case, Net Weight 27.00 lb
Category
Food
Distribution
3 states
HighFDA (Food)·F-0683-2025·2025-04-09
Lean Cuisine Ravioli Recalled Due to Potential Wood-Like Foreign Material
Nestle USA is recalling Lean Cuisine Spinach Artichoke Ravioli due to potential wood-like foreign material in the product. The affected 9-ounce frozen meals were distributed across 33 states.
Product
Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Food)·F-0709-2025·2025-04-09
Flaxseed Oil Dietary Supplement Recalled for Undeclared Soy Allergen
Bioriginal Food & Science Corporation recalls Fresh Flax Oil OMEGA 3-6-9 due to undeclared soy lecithin. Consumers with soy allergies should not consume this product.
Product
Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml, Dietary Supplement, Black HDPE plastic bottle with cap, Manufactured for Natural Slim, San Juan Puerto Rico
Category
Food
Distribution
1 state
HighFDA (Food)·F-0687-2025·2025-04-09
Julie's Gorditas De Nata Recalled for Undeclared Wheat Allergen
Julie's Gorditas De Nata is being recalled because the product label fails to declare wheat as an ingredient, posing a risk to consumers with wheat allergies. The recall affects 240 units distributed to two wholesalers.
Product
Julie's Gorditas De Nata; Ingredients: Flour, Vegetable Oil, Sugar, Baking Soda, Milk, Sour Cream, Butter, Cream Of Milk, Cinnamon, Vanilla; Net Wt. 16.75 OZ UPC# 0 00202 12018 6
Category
Food
Distribution
0 states
HighFDA (Food)·F-0693-2025·2025-04-09
Good & Gather Baby Vegetable Puree Recalled for Elevated Lead Levels
Good & Gather baby vegetable puree (4 oz) is being recalled due to elevated levels of lead. The recall affects 25,600 units distributed nationwide by Target.
Product
Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1. Distributed by Target Corporation, Minneapolis, MN 55403. Product of Colombia
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1475-2025·2025-04-09
Otopore Square Outer Ear Wound Dressing Recall for Sterility Seal Defect
Stryker Corporation is recalling Otopore Square outer ear wound dressings nationwide because sterile packaging seals may develop bubbles, indicating a potential breach of the sterile barrier. Consumers should stop using affected units and contact their healthcare provider.
Product
Otopore Square outer ear wound dressing, Firm Catalog Number 5400-020-100 and Forte Catalog Number 5400-020-100ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2025·2025-04-09
Hemopore nasal wound dressing packaging seal defect may compromise sterility
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Product
Hemopore 8cm nasal/sinus temporary wound dressing, Catalog Numbers 5400-020-208 and 5400-020-208ITL (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1489-2025·2025-04-09
Stryker Spine Monterey AL Implant Inserter Gold Unlock Button Separation Recall
Stryker Spine has recalled 56 units of the Monterey AL Implant Inserter due to potential separation of the gold unlock button. This could impair the device's function during surgical implant placement.
Product
Monterey AL Implant Inserter; 14/16mm; Catalog 48019120.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1482-2025·2025-04-09
Stryker nasal wound dressing recalled for defective sterile packaging seal
Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.
Product
Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2025·2025-04-09
Nasopore Standard Nasal Dressing Recalled Due to Sterility Seal Defects
Stryker is recalling 182,344 units of Nasopore Standard nasal dressings nationwide due to potential bubbles in blister seals that may breach the sterility barrier and increase contamination risk.
Product
Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0304-2025·2025-04-09
Tolterodine Tartrate Extended-Release Capsules Recalled for Failed Dissolution
Tolterodine Tartrate Extended-Release Capsules, 2 mg (Lot T05393) are being recalled because they failed dissolution specifications. The capsules may not dissolve as intended.
Product
Tolterodine Tartrate Extended-Release Capsules, 2 mg, 30 Capsules (3 x 10) Unit Dose carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6592-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0305-2025·2025-04-09
Sterile ophthalmic solution recalled for subpotent drug strength
Imprimis NJOF is recalling 2,822 bottles of sterile ophthalmic solution because stability testing showed subpotent drug strength below specifications.
Product
Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5 mL fill in 15 mL bottle, Imprimis NJOF, LLC, Route 46 West, Unit 6B, Ledgewood, NJ, 07852, NDC: 71384-733-05.
Category
Drug
Distribution
2 states
ModerateFDA (Devices)·Z-1503-2025·2025-04-09
Laboratory diagnostic reagent distributed with incorrect calibration value on package label
Fisher Diagnostics is recalling Pacific Hemostasis Thromboplastin-D reagent (1,699 units) due to an incorrect International Sensitivity Index (ISI) value printed on the box. No illnesses or injuries have been reported.
Product
Pacific Hemostasis Thromboplastin-D, 10 ml. Used in performing one-stage prothrombin time test and factor assays.
Category
Medical Device
Distribution
1 state
ModerateNHTSA·25V218000·2025-04-09
Alliance RV Avenue placards may show incorrect weight and capacity figures
Alliance RV is recalling certain 2025 Avenue 23ML travel trailers because the Federal Placard may show incorrect unloaded vehicle weight and cargo carrying capacity.
Product
ALLIANCE RV — ALLIANCE RV AVENUE
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0309-2025·2025-04-09
Prescription Antipsychotic Drug Recalled for Manufacturing Impurity
Glenmark Pharmaceuticals is recalling Chlorpromazine Hydrochloride Tablets due to a manufacturing quality deviation involving an impurity above recommended limits.
Product
CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1513-2025·2025-04-09
Surgical Suture Needles Recalled Due to Manufacturing Defect
Ethicon Endo Surgery recalls PDS PLUS VIO surgical sutures with needles due to silicone curing defects during manufacturing. 792 units were distributed worldwide.
Product
PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0307-2025·2025-04-09
Voriconazole Tablets Recalled Due to Manufacturing Practice Deviations
Amerisource Health Services is recalling Voriconazole 50 mg tablets distributed nationwide due to current Good Manufacturing Practice deviations related to repackaging.
Product
VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V222000·2025-04-08
Micro Bird Recalls 2023 G5 Transit Buses for Suspension Bolt Defect
Micro Bird is recalling 2023 G5 transit buses because u-bolts securing the suspension may break, increasing crash risk.
Product
MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E024000·2025-04-08
ILJIN Hysolus Recalls Compressed Natural Gas Tanks Due to Rupture Risk
ILJIN Hysolus is recalling specific CNG tanks because the pressure relief device may not fully vent, potentially causing the tank to rupture and increasing the risk of fire and injury.
Product
FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V223000·2025-04-08
Micro Bird Recalls 2023-2024 G5 School Buses for Suspension Bolt Defect
Micro Bird is recalling 2023-2024 G5 school buses because u-bolts securing the suspension may break, increasing crash risk.
Product
MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V219000·2025-04-08
White River Marine Recalls 2024-2025 Trailstar Boat Trailers Due to Winch Strap Defect
White River Marine Group is recalling 2024-2025 Trailstar TRL and Topper boat trailers because the winch strap may fray and break, allowing the boat to detach.
Product
TRAILSTAR — TRAILSTAR TOPPER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V214000·2025-04-08
Volvo Recalls 2023-2026 VNL Trucks for Hazard Switch Lighting Defect
Volvo Trucks North America is recalling 2023-2026 VNL trucks because the hazard switch back lighting may become inoperative, increasing crash risk.
Product
VOLVO — VOLVO VNL (4)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V220000·2025-04-08
Porsche Recalls Macan Electric Vehicles Due to Rearview Camera Software Defect
Porsche is recalling 2024-2025 Macan Electric vehicles because the rearview camera may display a blurry image or fail to display, increasing crash risk.
Product
PORSCHE — PORSCHE MACAN ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E023000·2025-04-08
Harley-Davidson Recalls Touring Motorcycles for Obstructed Reflectors
Harley-Davidson is recalling specific 2023-2025 Touring motorcycles because installed accessories may obstruct reflectors, reducing visibility to other road users.
Product
STRUCTURE:MOTORCYCLE:FAIRING/COWLING/WINDSCREEN recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V213000·2025-04-07
2022–2023 Nova Bus LFS Transit Buses Engine Wiring Harness Recall
Nova Bus is recalling certain 2022–2023 LFS transit buses because the engine wiring harness may be incorrect length, risking harness damage and loss of drive power that could cause a crash.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·011-2025·2025-04-05
Johnsonville Recalls Cheddar Bratwurst Due to Possible Hard Plastic Contamination
Johnsonville is recalling approximately 22,672 pounds of cheddar bratwurst sold in ten states due to possible hard plastic contamination. No injuries have been reported.
Product
Momence Real Estate — Johnsonville, LLC, Recalls Cheddar Bratwurst Product Due to Possible Foreign Matter Contamination
Category
Food
Distribution
10 states
HighNHTSA·25V212000·2025-04-04
Forest River Recalls 2025 Coachmen Travel Trailers Due to Solar Wiring Fire Risk
Forest River is recalling 2025 Coachmen Apex and Remote travel trailers because incorrect solar panel wiring may melt and cause a fire.
Product
COACHMEN — COACHMEN APEX, REMOTE
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25208·2025-04-03
Polaris RZR Pro R and Pro R 4 recalled for ROPS fastener defect
Polaris is recalling about 910 RZR Pro R and Pro R 4 recreational off-road vehicles (2022-2025) due to missing or loose fasteners on the rollover protective structure that can fail to protect occupants in a rollover or tip-over.
Product
Model Year 2022-2025 RZR Pro R and RZR Pro R 4 Recreational Off-Road Vehicles (ROVs)
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25204·2025-04-03
USB-Powered LED Bear Lights Recalled for Fire and Burn Hazards
Five Below is recalling about 29,000 LED Iridescent Bear Lights because the USB power switch can overheat and melt. The company received 28 reports of overheating, including 6 finger burns and 2 property damage incidents.
Product
Room2Room LED Iridescent Bear Lights
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25V207000·2025-04-03
Starcraft RV Recalls 2025 Autumn Ridge Travel Trailers Due to Safety Chain Defect
Starcraft RV is recalling 2025 Autumn Ridge travel trailers because the installed safety chains are rated below the vehicle's Gross Vehicle Weight Rating, creating a risk of trailer separation.
Product
STARCRAFT RV TT — STARCRAFT RV TT AUTUMN RIDGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V206000·2025-04-03
Blue Arc BA4L-800 Recall for Battery Seal Defect
Shyft Group is recalling 2025 Blue Arc BA4L-800 vehicles because improperly sealed battery packs may allow liquid entry, increasing fire and shock risks.
Product
BLUE ARC — BLUE ARC BA4L-800
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V209000·2025-04-03
Autocar Recalls 2023-2024 Legend Vehicles Due to Brake System Defect
Autocar is recalling 2023-2024 Legend vehicles because air tanks have insufficient volume, which can reduce brake function and increase crash risk.
Product
AUTOCAR — AUTOCAR LEGEND
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V208000·2025-04-03
Autocar Recalls Legend Vehicles Due to Incorrect Blower Motor Fuse
Autocar is recalling 2020-2026 Legend vehicles because an incorrect blower motor fuse may fail to trip, increasing the risk of a fire.
Product
AUTOCAR — AUTOCAR LEGEND
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25207·2025-04-03
Honda Recalls Accessory Heaters for Side-by-Side Vehicles Due to Fire Hazards
Honda is recalling about 2,340 aftermarket accessory heaters for Pioneer and Talon side-by-side vehicles because they can overheat and catch fire. The company has received three reports of overheating, including two that resulted in fires and vehicle damage.
Product
Accessory Heaters for Model Years 2022-2024 Honda Pioneer 1000, 2023-2025 Pioneer 700, and 2022-2024 Honda Talon 1000 Side-by-Side vehicles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25205·2025-04-03
Superb Sports Baby Bath Seats Recalled for Drowning and Tip-Over Hazard
Superb Sports baby bath seats sold on Amazon can tip over while in use, posing a drowning hazard to infants. No injuries have been reported.
Product
Superb Sports Baby Bath Seats
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25206·2025-04-03
HONEYJOY High Chairs Recalled for Suffocation Risk from Incline Violation
HONEYJOY Convertible and Foldable High Chairs are being recalled because they were marketed for infant sleep with an incline angle exceeding 10 degrees, violating federal safety regulations. About 2,750 units sold exclusively on Amazon from April 2023 to August 2024 are affected.
Product
HONEYJOY Convertible and Foldable High Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25203·2025-04-03
DEWALT 70,000 BTU Outdoor Propane Heaters Recalled for Fire and Burn Hazards
About 21,250 DEWALT 70,000 BTU outdoor propane heaters are being recalled due to operating instructions that can prevent proper fan operation, causing overheating and fire and burn hazards. No injuries have been reported.
Product
DEWALT 70,000 BTU Outdoor Portable Cordless Forced Air Propane Heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25212·2025-04-03
Ashland Casement Window Hinge Tracks Recalled for Impact Injury Hazard
Amesbury Industries is recalling about 200,000 Ashland casement window hinge tracks because the metal sliding arm can disengage, causing the window sash to fall and creating an impact injury hazard. No injuries have been reported.
Product
Ashland 10-inch and 14-inch two-bar casement window hinge tracks
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25209·2025-04-03
Foldable Travel Hair Dryers Recalled Due to Electrocution and Shock Hazards
AliExpress is recalling about 80 foldable travel hair dryers sold from April 2022 through January 2025 because they lack immersion protection and can cause electrocution or shock if they fall into water while plugged in. No injuries have been reported.
Product
Foldable Travel Hair Dryers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V184000·2025-04-03
Nova Bus LFS Transit Buses Recalled for Battery Fire Risk
Nova Bus is recalling 2022-2023 LFS transit buses because high voltage battery hardware may come loose and cause a short circuit, creating a fire risk.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25210·2025-04-03
Mini travel hair dryers recalled for electrocution and shock hazard
XZT mini hair dryers sold on AliExpress lack immersion protection and can cause electrocution or shock if they fall into water while plugged in. No injuries have been reported.
Product
Mini Travel Hair Dryers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25211·2025-04-03
LVOE Hair Dryers Recalled for Electrocution and Shock Hazards
AliExpress is recalling LVOE-brand hair dryers sold from April 2023 through December 2024 because they lack immersion protection and can cause electrocution if they fall into water while plugged in. No injuries have been reported.
Product
LVOE Hair Dryers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V210000·2025-04-03
Honda Recalls 2018-2025 CB300R Motorcycles for Headlight Flickering Defect
Honda is recalling 2018-2025 CB300R motorcycles because headlights may flicker or shut off while driving, increasing crash risk.
Product
HONDA — HONDA CB300R
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25214·2025-04-03
Vivitar Blender Bottles Recalled by Sakar for Laceration Hazard
Sakar International is recalling about 199,000 Vivitar Blender Bottles sold at Target because the blades can continue operating when the bottle is removed from the base. No injuries have been reported.
Product
Vivitar Blender Bottles
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0300-2025·2025-04-02
SinuCleanse Nasal Saline Packets Recalled for Bacterial Contamination
SinuCleanse Premixed Saline Packets sold nationwide are being recalled due to contamination with Staphylococcus aureus, a bacterium that can cause infection.
Product
SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg) for Nasal Wash System, 60-count All Natural USP Grade Saline Packets, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00103 4
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V205000·2025-04-02
Jayco Recalls 2024-2025 Entegra Motorhomes Due to Fuel Hose Separation
Jayco is recalling 2024-2025 Entegra Anthem, Aspire, and 2025 Reatta XL motorhomes because a fuel hose may separate, causing a leak, fire, or engine stall.
Product
ENTEGRA — ENTEGRA ANTHEM, ASPIRE, REATTA XL
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0669-2025·2025-04-02
Glicks Dark Chocolate Conettos recalled for undeclared milk allergen
Kenover Marketing Corp. is recalling Glicks Dark Chocolate Conettos due to an undeclared milk allergen. The product was distributed across multiple states. Consumers with milk allergies should not consume it.
Product
Glicks Dark Chocolate Conettos, 2.47 oz., Plastic Bag, 24 packages per case
Category
Food
Distribution
10 states
SevereFDA (Food)·F-0673-2025·2025-04-02
Wangzhine Hot Pot Sauce Recalled for Undeclared Wheat and Soy Allergens
Wangzhine branded Hot Pot Sauce (SPICY) is recalled for undeclared Wheat and Soy allergens. The affected product poses a risk to consumers with these allergies.
Product
Wangzhine branded Hot Pot Sauce (SPICY); Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001382
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0299-2025·2025-04-02
SinuCleanse Nasal Wash System Recalled for Bacterial Contamination
Ascent Consumer Products Inc. is recalling SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System nationwide due to bacterial contamination with Staphylococcus aureus. Affected lot number is 024122661Al with expiration date 12/2027.
Product
SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 Soft tip Squeeze Bottle, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1396-2025·2025-04-02
CVAC Aspiration System Requires Labeling Update for Pressure Risk
The CVAC Aspiration System requires a labeling update to add safety instructions for high-viscosity kidney fluid. Continuing fluid inflow without adequate outflow can create dangerous intrarenal pressure imbalances.
Product
CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of urinary tract and kidney interior.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0663-2025·2025-04-02
Jinga Glass Noodles Recalled for Undeclared Egg Allergen
HAR Maspeth Corp. is recalling Jinga Glass Noodles for containing undeclared egg. The product, distributed across the Northeast and Midwest, poses a risk to consumers with egg allergies.
Product
Jinga Glass Noodles with vegetables 8 oz. and 12 oz.
Category
Food
Distribution
10 states
SevereFDA (Food)·F-0672-2025·2025-04-02
Wangzhine Hot Pot Sauce recalled for undeclared wheat and soy allergens
Liaoning Cheng Da (USA) Inc is recalling Wangzhine branded Hot Pot Sauce due to undeclared wheat and soy allergens. The recall affects 3,650 cases distributed to 5 direct accounts in California.
Product
Wangzhine branded Hot Pot Sauce; Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001375
Category
Food
Distribution
1 state
SevereUSDA FSIS·010-2025·2025-04-02
Hearthside Recalls Breakfast Sandwiches for Undeclared Sesame Allergen
Hearthside Food Solutions is recalling approximately 489,887 pounds of ready-to-eat breakfast sandwiches because they contain sesame, a known allergen, that is not declared on the label.
Product
Hearthside Food Solutions LLC d/b/a Maker's Pride — Hearthside Food Solutions, LLC Recalls Ready-To-Eat Sausage and Bacon Breakfast Sandwiches Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0301-2025·2025-04-02
SinuCleanse Neti Pot Nasal Wash System Recalled for Bacterial Contamination
Ascent Consumer Products Inc. is recalling SinuCleanse Soft Tip Neti Pot Nasal Wash System due to bacterial contamination with Staphylococcus aureus. Consumers should stop using this product immediately.
Product
SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 kettle style Neti Pot, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1390-2025·2025-04-02
Shiley Adult Tracheostomy Tubes Recalled Due to Flange Disconnection Risk
Covidien is recalling 780 Shiley Adult Flexible Tracheostomy Tubes because the flange may disconnect from the outer cannula, potentially causing respiratory failure, aspiration, or death.
Product
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula, REF: 7CN80R
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1465-2025·2025-04-02
Medline procedure kits with defective plastic syringes recalled due to leak and breakage risk
Medline procedure kits containing plastic syringes are being recalled due to leaks, breakage, and quality issues that may compromise sterile medical procedures. Approximately 14,589 units were distributed nationwide in the US and Canada.
Product
Medline procedure kits labeled as: 1) ACL ARTHROSCOPY PACK, Pack Number DYNJ55316G; 2) ARTERIOGRAM PACK, Pack Number DYNJ64332; 3) ARTHRO PACK-LF, Pack Number DYNJ38748F; 4) ARTHRO PACK-LF, Pack Number DYNJ38748F; 5) ARTHROGRAM PACK, Pack Number DYNJ65817; 6) ARTHROGRAM TR
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1441-2025·2025-04-02
Medline Surgical Procedure Kits Recalled for Syringe Leakage and Breakage
Medline Industries has recalled 11,774 surgical procedure kits with defective plastic syringes that may leak or break. The kits were distributed nationwide and in Canada.
Product
Medline procedure kits labeled as: 1) ABLATION PACK, Pack Number DYNJ40629B; 2) ACH LAPAROSCOPIC GB PACK, Pack Number DYNJ67756A; 3) CHRISTUS WH LAP CHOLE PACK, Pack Number DYNJ60934B 4) CRMC LAP CHOLE DIAG LAP-LF, Pack Number DYNJ61095D; 5) CYSTO PACK, Pack Number DYNJ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1464-2025·2025-04-02
Medline Procedure Kits Recalled for Syringe Quality Defects
Medline procedure kits with defective plastic syringes have been recalled due to leaks, breakage, and quality issues that may pose a risk to patient health. The recall involves 422 units distributed in the US and Canada.
Product
Medline procedure kits labeled as: 1) ACOUSTIC NEUROMA PACK-LF, Pack Number DYNJ37741B; 2) ANGIOGRAPHY PACK, Pack Number DYNJ21519W; 3) NEURO ANGIO PACK, Pack Number DYNJ83941; 4) NEURO ANGIO PACK SJF-LF, Pack Number DYNJ55678; 5) NEURO PACK, Pack Number DYNJ04851Q;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1438-2025·2025-04-02
Medline Surgical Procedure Kits Recalled for Defective Plastic Syringes
Medline Industries recalls 3,860 surgical procedure kits with defective plastic syringes that may leak or break during use. The affected kits are distributed in the US and Canada.
Product
Medline procedure kits labeled as: 1) AV FISTULA PACK, Pack Number DYNJ80088; 2) AV FISTULA PACK-LF, Pack Number DYNJ0131782J; 3) CABG, Pack Number DYNJ906462B; 4) CABG ACCESSORY PACK-LF, Pack Number DYNJ0261346U; 5) CARDIAC CATH PACEMAKER-LF, Pack Number DYNJ42997C;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1419-2025·2025-04-02
Baxter TruSystem 7500 Software Issue Impairs Upper Back Adjustment in Emergency Mode
Baxter Healthcare is recalling 93 TruSystem 7500 Hybrid Plus units for a software issue that renders the upper back section inoperable when emergency mode is enabled.
Product
Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1425-2025·2025-04-02
Lap Pack Convenience Kits Recalled for Sterility Assurance Concerns
American Contract Systems is recalling 500 Lap Pack - 170307 convenience kits distributed in Arizona due to sterility assurance concerns with procedure trays.
Product
Brand Name: Banner Health Systems Product Name: Lap Pack - 170307 Model/Catalog Number: BHLP62H Software Version: N/A Product Description: Convenience Kit Component: No
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1430-2025·2025-04-02
Pressure Monitoring Lines Recalled for Manufacturing Defect in Luer Fittings
Medline Industries is recalling namic medical convenience kits containing Pressure Monitoring Lines with defective female luer fittings manufactured with excess material. The defect could impair device function.
Product
namic convenience kits labeled as: MTS,COLOR,PML,KIT,-,FRENCH HOSPITAL PG; medical convenience kit, REF 600605710
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1439-2025·2025-04-02
Medline Procedure Kits With Defective Plastic Syringes Recalled
Medline is recalling surgical procedure kits with plastic syringes affected by a March 2024 FDA Safety Alert due to leaks, breakage, and quality issues that may pose risks to patients.
Product
Medline procedure kits labeled as: 1) AV FISTULA PACK-LF, Pack Number DYNJ0826753O; 2) BARRINGTON ACCESSORY TTL KNEE, Pack Number DYNJ56717A; 3) CVL INSERTION PACK, Pack Number CVI5065; 4) KT DR VELASCO FISTULA PACK, Pack Number DYNJ46648D; 5) PICC ABSCESS PACK-LF, Pac
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1447-2025·2025-04-02
Medline procedure kits recalled for syringe quality defects
Medline Industries is recalling 1,711 procedure kits containing plastic syringes affected by manufacturing defects. The syringes may leak or break, posing a risk to patient safety during medical procedures.
Product
Medline procedure kits labeled as: 1) CLOVIS ROBOTIC-LF, Pack Number DYNJ61061D; 2) CSMC/GYN LAPAROSCOPIC PACK-LF, Pack Number DYNJ0665103I; 3) DAVINCI PACK-RFD, Pack Number DYNJ47762O; 4) DAVINCI ROBOT PACK SLRMC, Pack Number DYNJ81236; 5) GENERAL ROBOTICS PACK, Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1423-2025·2025-04-02
Baxter NovumIQ Syringe Infusion Pumps Recalled for Gasket Defect Risk
Baxter Healthcare is recalling 149 NovumIQ syringe infusion pumps with incorrectly installed gaskets that could allow fluid ingress during cleaning or after IV fluid spills.
Product
Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1463-2025·2025-04-02
Medline medical procedure kits recalled for plastic syringe defects
Medline procedure kits with plastic syringes are being recalled due to potential leaks and breakage that may affect patient safety. The recall impacts 1152 units distributed nationwide and in Canada.
Product
Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1431-2025·2025-04-02
Medline Pressure Monitoring Kits Recalled for Luer Fitting Manufacturing Defect
Medline Industries is recalling 1,669 pressure monitoring line convenience kits distributed worldwide. The female luer fittings contain excess material near the fluid pathway.
Product
namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS,ST. *, REF 60010511; 3) MTS,LT,HT,KIT-BRYAN,LGH,M.C.,EAST, REF 60020323; 4) MTO,RIGHT,KIT-BRONSON,M* HOSP PG, REF 60020676; 5) MTS,LEFT HEART,KIT-C*,ME
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1446-2025·2025-04-02
Medline Delivery and Labor Kits Recalled for Defective Plastic Syringes
Medline is recalling 1,958 delivery and labor procedure kits containing plastic syringes with leaks, breakage, and quality defects that may pose a risk to patient health.
Product
Medline procedure kits labeled as: 1) DELIVERY PACK, Pack Number DYNJ0923016; 2) DELIVERY PACK-LF, Pack Number DYNJ0968863M; 3) L & D PACK-LF, Pack Number DYNJ0373290N; 4) L&D PACK, Pack Number DYNJ51998A; 5) LABOR & DELIVERY PACK-LF, Pack Number DYNJ0348455P; 6) LAB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1454-2025·2025-04-02
Helix Elite Quality Control Material Recalled for Delayed Detection and QC Failure
Microbiologics Inc is recalling its Helix Elite RSV quality control material (Lot HE0044-131) because the RSV component may produce delayed test results and could fail quality control checks. This Class II recall affects 28 units distributed worldwide.
Product
Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory Syncytial Virus, Multi-analyte, unassayed quality control material, Catalog Number HE0044N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1449-2025·2025-04-02
Medline Procedure Kits With Defective Syringes Recalled Nationwide
Medline is recalling 268 procedure kits nationwide due to plastic syringes affected by a March 2024 FDA safety alert. The syringes may leak, break, or have quality issues that could affect patient care.
Product
Medline procedure kits labeled as: 1) CSMC/ABDOMINAL HYST PACK-LF, Pack Number DYNJ0665086F; 2) MAJOR VAGINAL HARPER PACK-LF, Pack Number DYNJ0161768D; 3) ROBOT LAP TOTAL HYST, Pack Number DYNJ907811A; 4) VAG HYSTE PACK-LF, Pack Number DYNJ0773613J; 5) VAG HYSTERECTOMY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1467-2025·2025-04-02
Checkpoint Guardian Intraoperative Lead: Potential Electrical Exposure Risk
Adhesive may not fully encapsulate metallic components on Checkpoint Guardian Intraoperative Leads, creating potential for electrical current leakage. This could cause inconsistent muscle responses and incorrect surgical actions.
Product
Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraoperative Lead, Medium Model/Catalog Number: REF# 9525 (Medium) Product Description: The Checkpoint Guardian Intraoperative Leads are single-patient disposable accessories for providing
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1414-2025·2025-04-02
Baxter TruSystem 7500 U Medical Device Software Malfunction Recall
Baxter is recalling the Stationary column TruSystem 7500 U due to a software issue that prevents the upper back section from being adjustable when emergency mode is enabled.
Product
Baxter Stationary column TruSystem 7500 U, Product Code 1730731
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1468-2025·2025-04-02
Progressa bed surfaces recalled for mattress dips when head elevated
Baxter Healthcare's Progressa Bed Surfaces may develop dips in the mattress when the head of the bed is elevated, as air bladders inside can shift out of position. This could reduce the bed's effectiveness at preventing pressure ulcers.
Product
Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1450-2025·2025-04-02
Medline Medical Procedure Kits With Plastic Syringes Recalled for Quality Issues
Medline medical procedure kits containing plastic syringes are being recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health.
Product
Medline procedure kits labeled as: 1) L S GYN PACK, Pack Number DYNJ65616C; 2) MAIN CYSTO, Pack Number DYNJ61371A; 3) OB PACK-LF, Pack Number DYNJ20720C; 4) PELVISCOPY PACK-LF, Pack Number DYNJ0415776N; 5) POSTERIOR EYE PACK-LF, Pack Number PHS656483I; 6) ROBOTICS PA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1462-2025·2025-04-02
Medline Surgical Procedure Kits Recalled for Defective Plastic Syringes
Medline Industries is recalling 1,228 surgical procedure kits containing defective plastic syringes. The syringes may leak or break during use, potentially affecting patient safety.
Product
Medline procedure kits labeled as: 1) BREAST PACK-LF, Pack Number DYNJ0956628O; 2) BREAST SURGERY FOAKS, Pack Number DYNJ63577C; 3) CHEST BREAST -LF, Pack Number DYNJCEN04C; 4) DIEP PACK, Pack Number DYNJ60669G; 5) FACE LIFT PACK, Pack Number DYNJ64670B; 6) FREE FLAP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1411-2025·2025-04-02
Baxter surgical table software issue blocks emergency back adjustment
Baxter is recalling 112 units of the TruSystem 7500 surgical table due to a software issue preventing upper back adjustment during emergency mode. No injuries have been reported.
Product
Baxter Floor mounting column TruSystem 7500, Product Code 1717021
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1413-2025·2025-04-02
Baxter Mobile column TruSystem 7500 U emergency mode software issue affects back adjustment
A software issue in the Baxter Mobile column TruSystem 7500 U prevents the upper back section from being operable or adjustable when emergency mode is enabled. Approximately 40 units distributed nationwide are affected.
Product
Baxter Mobile column TruSystem 7500 U, Product Code 1730720
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1442-2025·2025-04-02
Medline General Endoscopy Procedure Kit Recalled Due to Syringe Defects
Medline is recalling General Endoscopy procedure kits due to plastic syringe defects that may leak or break. The affected kits pose potential risk to patient health during medical procedures.
Product
Medline procedure kits labeled as: 1) GENERAL ENDOSCOPY PACK, Pack Number DYNJ44673G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1444-2025·2025-04-02
Medline surgical procedure kits recalled for syringe leaks and breakage
Medline procedure kits containing plastic syringes are recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health. The affected kits were distributed nationwide in the US and Canada.
Product
Medline procedure kits labeled as: 1) A & A KNEE PACK-LF, Pack Number DYNJHS0136D; 2) ABD CLOSURE PACK, Pack Number DYNJ56987B; 3) ADULT PERC PACK-LF, Pack Number PHS170994005A; 4) BASIC PACK, Pack Number DYNJ54836B; 5) BASIC PACK, Pack Number DYNJ58678A; 6) BASIC PACK, Pa
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1437-2025·2025-04-02
Medline Procedure Kits Recalled Due to Defective Plastic Syringe Quality Issues
Medline is recalling 9,246 units of medical procedure kits containing defective plastic syringes with leaks and breakage that may pose a risk to patient health. The kits were distributed nationwide in the US and in Canada.
Product
Medline procedure kits labeled as: 1) ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D; 2) ANGIO PACK, Pack Number DYNJ69678; 3) ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A; 4) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C; 5) ANGIOGRAPHY PACK, Pack Number DYNJ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1409-2025·2025-04-02
Baxter Operating Table Column Software Issue Limits Emergency Mode Function
Baxter Healthcare is recalling 403 TS7500 MOBIUS operating table columns due to a software issue that prevents the upper back section from being adjustable when emergency mode is activated.
Product
Baxter Operating table column TS7500 MOBIUS, Product Code 1704695
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0293-2025·2025-04-02
Strides Pharma Testosterone Gel Recalled Due to Benzene Contamination
Strides Pharma is recalling Testosterone Gel 1% (195,952 cartons nationwide) due to benzene contamination. Consumers using affected lots should immediately contact their healthcare provider.
Product
TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0294-2025·2025-04-02
Testosterone Gel Recalled Nationwide Due to Benzene Contamination
Strides Pharma is recalling Testosterone Gel 1% nationwide due to the presence of benzene, a toxic substance. Patients should contact their healthcare provider about alternative treatment options.
Product
TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
Category
Drug
Distribution
Distributed nationwide

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