Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent Product Recall Alerts List
Showing 3,076 - 3,100 of 4,622 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
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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 to the central circulation.
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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FDA
Z-1916-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 11, 2026
|
Details |
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Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes JUDKINS PACK DYNJ51126 ANGIO PACK DYNJ32555C, DYNJ66631 ANGIO TRAY DYNJ46153B ANGIOGRAPHY PACK DYNJ26855F ANGIOGRAPHY PACK-M-LF DYNJ24530I ANGIOGRAPHY TRAY-LF DYNJ0220880V, DYNJ30077D CATH LAB ANGIO PACK-LF DYNJ0545064X CATH LAB PACK DYNJ39057C FEMORAL ANGIOGRAPY SET UP DYNJ61015B RAD-ANGIO PACK DYNJ47710C SURGERY ANGIO PACK-LF PHS677784013A
Unapproved design changes to the products outside of the 510(k) clearance.
|
FDA
Z-1876-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
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Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.
Potential for detachment of a distal tip component of the device during use.
|
FDA
Z-1851-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 23, 2026
|
Details |
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Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UPN No.: H787107140215 (Box), H787107140210 (Pouch); Box Quantity: 5 pouches;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
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FDA
Z-1866-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
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Details |
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Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BASIC CL PACK-LF DYNJ87052 BASIC PACK DYNJ83976 BASIC SET UP PACK DYNJ80700 CORONARY ANGIOGRAPHY PACK (N) DYNJ42136B CSTM ANGIO KIT - S VASC1109 CV PACK DYNJ46301C DR F PACK DYNJ41253B ENSEMBLE HEMORROIDES DYNJ56311A G TAVR PACK DYNJ61006 IR MINOR PACK DYNJ44139C MAJOR PLUS PACK DYNJ905160N MAXIMUM BARRIER BUNDLE PACK DYNJ35216C PCI PACK TBRHSC-LF DYNJ41941D PERC PACK-LF DYNJ0774759P PERIPHERAL ANGIOGRAPHY PK DYNJ42094B PR
Unapproved design changes to the products outside of the 510(k) clearance.
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FDA
Z-1883-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
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LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
|
FDA
Z-1930-2026
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Medical Device | High |
Apr 29, 2026
Recall: Mar 9, 2026
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Details |
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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;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
|
FDA
Z-1863-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
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Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B ANGIO PHC DYNJ37485C C.I.C.N. ANGIO PACK DYNJ53064B FHT P NEURO PACK DYNJ39931D NEURO ARTERIOGRAM PACK-LF DYNJ0948060F NEURO KIT NAM0003 NEURO PACK DYNJ61542D NEURO RADIOLOGY PACK DYNJ59903B NEURO TRAY DYNJ84872A PK, CATH LAB-ANGIO DYNJ44027F QVH IR NEURO PACK DYNJ62176
Unapproved design changes to the products outside of the 510(k) clearance.
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FDA
Z-1884-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
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Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK, Model Number: DYNJT2021G; 3) ANGIOGRAPHY PACK, Model Number: DYNJ31377B; 4) ANGIO PACK, Model Number: DYNJ51279; 5) ANGIOGRAPHY PACK II, Model Number: DYNJ52447; 6) CATH ANGIO PACK, Model Number: DYNJ53369C; 7) ANGIO PACK, Model Number: DYNJ53591A; 8) ANGIOGRAPHIC PACK, Model Number: DYNJ57516; 9) ANGIOGRAPHY TRAY-LF, Model Number: DYNJ58722A; 10) ANGIO TRAY W/CHLORAPREP, Model Number: DYNJ62742; 11) CEREBRAL ANGIOGRAM, Model Number: DYNJ67876; 12) CSU CATH MANIFOLD KIT, Model Number: VASC1170A
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1834-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
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Details |
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Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF, Model Number: DYNJT2164M; 4) ANGIOGRAPHY TRAY, Model Number: DYNJT3078; 5) CATH PACK, Model Number: DYNJT4190; 6) ANGIO VASCULAR PACK, Model Number: DYNJT5717; 7) HEART CATH PACK, Model Number: DYNJ0381139R; 8) CARDIAC CATH PACK, Model Number: DYNJ04529L; 9) CUSTOM RADIOLOGY PACK, Model Number: DYNJ07955L; 10) STVZ CARDIAC CATH PACK, Model Number: DYNJ24619J; 11) CATH TRAY #2, Model Number: DYNJ24706D; 12) CATH LAB PACK, Model Number: DYNJ24802Q; 13) CATH PACK, Model Number: D
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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FDA
Z-1835-2026
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Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
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Details |
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LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
|
FDA
Z-1933-2026
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Medical Device | High |
Apr 29, 2026
Recall: Mar 9, 2026
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Details |
|
FDA
Z-1903-2026
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Medical Device | High |
Apr 29, 2026
Recall: Mar 25, 2026
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Details | |
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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;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
|
FDA
Z-1873-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
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Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG S, Model Number: DYNJHWIRE105; 3) GWIRE HYDRO 0.035 260CM ANG S, Model Number: DYNJHWIRE107; 4) GWIRE HYDRO 0.035 260CM STR S, Model Number: DYNJHWIRE115; 5) GWIRE HYDRO 0.035 150CM STR, Model Number: DYNJHWIRE108; 6) GWIRE HYDRO 0.035 150CM ANG S, Model Number: DYNJHWIRE104; 7) GWIRE HYDRO 0.035 180CM STR S, Model Number: DYNJHWIRE113; 8) GWIRE HYDRO 0.035 260CM ANGLE, Model Number: DYNJHWIRE103; 9) GDWIRE .035INX150CM 3MMJ LT, Model Number: DYNJGWIRE01L; 10) GDWIRE .035INX18
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1829-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC.
Potential for detachment of a distal tip component of the device during use.
|
FDA
Z-1854-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 23, 2026
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Details |
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Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes TAVR PACK DYNJ69246B ABDOMINAL VASCULAR-LF DYNJ905291D ANGIOGRAPHIC PACK DYNJ86769 AORTAGRAM PACK DYNJ26783D AV FISTULA PACK CHS-LF DYNJ35615G AV SHUNT PACK-LF DYNJ0842516G CATHETER PACK DYNJ61926 EP DRAPE PACK-LF DYNJ47645C EP PACK DYNJ47782G EPS ACCESSORY PACK DYNJT2201S H CLINIC VASCULAR PK DYNJ33415A HEART FAILURE PACK DYNJ64877B HYBRID PACK DYNJ65925D INTERVENTIONAL RAD PACK DYNJ44100M INTERVENTIONAL RADIOLOGY PK-LF DYNJ0516014AG MV-PACEMAKER PACK-LF DYNJ41556F NEURO RADIOLOGY RICHMOND DYNJ68365D OR HYB
Unapproved design changes to the products outside of the 510(k) clearance.
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FDA
Z-1878-2026
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Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
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Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ909398A ROBOTIC PACK DYNJ908706D
Unapproved design changes to the products outside of the 510(k) clearance.
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FDA
Z-1885-2026
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Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
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Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model Number: DYNJ37543A
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1838-2026
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Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (Box), H787107140140 (Pouch); Box Quantity: 5 pouches;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
|
FDA
Z-1862-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
Pop-Top Latch and Safety Straps May Fail
Roadtrek Inc. (Roadtrek) is recalling certain 2024-2026 Westfalia Wave SL, 2022-2026 Zion Slumber, Play Slumber, 2026 Play Tuff SL, 2025-2026 Play+Slumber, and 2024 Pivot Slumber recreational vehicles. The pop-top latch may disengage during transit, causing the pop-top to lift. A pop-top that lifts during transit can distract the driver, or detach if the secondary safety straps fail, increasing the risk of a crash.
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NHTSA
26V271000
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Vehicle | High |
Apr 29, 2026
Recall: Apr 29, 2026
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Details |
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Front Chin Spoiler May Detach During Transit
Newmar Corporation (Newmar) is recalling certain 2026 Freedom Aire motorhomes. The front chin spoiler may detach during transit. A detached spoiler may become a road hazard, increasing the risk of a crash.
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NHTSA
26V272000
|
Vehicle | High |
Apr 29, 2026
Recall: Apr 29, 2026
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Details |
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Incorrect Cargo Carrying Capacity on Label/FMVSS 120
Newmar Corporation (Newmar) is recalling certain 2026 Freedom Aire motorhomes. The Cargo Carrying Capacity (CCC) label may state an incorrect weight value. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, “Wheels and Rims - Other Than Passenger Cars.” Incorrect weight information can allow the vehicle to be overloaded, increasing the risk of a crash.
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NHTSA
26V273000
|
Vehicle | High |
Apr 29, 2026
Recall: Apr 29, 2026
|
Details |
|
Detached Shift Cable Bushing/FMVSS 102, 114
Dorman Products, Inc. (Dorman) is recalling certain Dorman Transmission Gearshift Cables, with part numbers 905-146, 905-644, 905-142, and Solutions Transmission Gearshift Cables with part numbers BK905-1146-1, and BK905-1142-1. The gearshift cable bushing may detach from the linkage, which can prevent the vehicle from shifting into gear properly, including "Park" position. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) numbers 102, “Transmission shift position sequence, starter interlock, and transmission braking effect," and FMVSS number 114, "Theft Protection." The inability to shift into "Park" can result in a vehicle rollaway, increasing the risk of a crash.
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NHTSA
26E024000
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Vehicle | High |
Apr 29, 2026
Recall: Apr 29, 2026
|
Details |
|
Improperly Routed Coolant Lines May Cause a Loss of Drive Power
Storyteller Overland, LLC (Storyteller) is recalling certain 2023 Stealth, Classic, and Beast Mode vehicles equipped with AWD. Improperly routed coolant lines may overheat the engine, causing a loss of drive power. A loss of drive power increases the risk of a crash.
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NHTSA
26V274000
|
Vehicle | High |
Apr 29, 2026
Recall: Apr 29, 2026
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Details |
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Loose Bolt in Front Seat Frame
Ford Motor Company (Ford) is recalling certain 2024-2026 Ranger and Bronco vehicles. The front seats may have a loose or dislodged seat frame height-adjust pivot bolt. A seat with a dislodged bolt may not properly restrain an occupant in a crash, increasing the risk of injury.
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NHTSA
26V268000
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Vehicle | High |
Apr 28, 2026
Recall: Apr 28, 2026
|
Details |
Recent Product Recall Alerts
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Latest Product Recalls FAQ
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