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 3,001 - 3,025 of 4,622 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
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Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog No.: 10714018; Product/UPN No.: H787107140185 (Box), H787107140180 (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-1865-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
Medline Kits: 1) PICC TRAY, Model Number: DYNJ41648A
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1837-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB 0SH; Catalog No.: 10714024; Product/UPN No.: H787107140245 (Box), H787107140240 (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-1867-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
|
FDA
Z-1807-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 6, 2026
|
Details |
|
Flamingo Funnel Large, Model Number SQ20012-03
Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.
|
FDA
Z-1926-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 16, 2026
|
Details |
|
Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; Catalog No.: 10731401; Product/UPN No.: H787107314015 (Box), H787107314010 (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-1869-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 18mm-19mm-20mm, REF 1205-20
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
|
FDA
Z-1941-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 18, 2026
|
Details |
|
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 12mm-13.5mm-15mm, REF 1205-15
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
|
FDA
Z-1939-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 18, 2026
|
Details |
|
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.
In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
|
FDA
Z-1808-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 6, 2026
|
Details |
|
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
|
FDA
Z-1899-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 25, 2026
|
Details |
|
LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
|
FDA
Z-1931-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 9, 2026
|
Details |
|
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADD A ENDOVASCULAR PACK-LF DYNJ0429339L, DYNJ0429339M ANGIO ARTERIOGRAM PACK-LF DYNJ0774026K ANGIO KIT PACK DYNJ83746B ANGIO TRAY NO LIDO DYNJ85557A ANGIOGRAPHY PACK II DYNJ17218S, DYNJ17218T ARTERIOGRAM NEURO PACK-LF DYNJ0842499L ARTERIOGRAM PACK-LF DYNJ0842478M CARDIAC CATH II PK DYNJ21259O CARDIAC CATH PACK DYNJ68653D CATH LAB ANGIOGRAPHY PACK DYNJ50779G CATH LAB-LF DYNJ51423G CRANIOTOMY PACK-LF DYNJ0101292I DEEP BRAIN STIMULATION PACK DYNJ0842793I ENDO VASCULAR MINOR DYNJ87263 GENERAL ENDO PACK-LF DYNJ08
Unapproved design changes to the products outside of the 510(k) clearance.
|
FDA
Z-1890-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
|
Medline Kits: 1) SYR CONTROL 8ML ROTATING, Model Number: DNSC89369; 2) SYRINGE 10ML CONTROL MLL, Model Number: DYNJSYR10C
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1843-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 25cm. Model Number: TB2-0525FC.
Potential for detachment of a distal tip component of the device during use.
|
FDA
Z-1852-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 23, 2026
|
Details |
|
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OER-ELITE.
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
|
FDA
Z-1898-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 25, 2026
|
Details |
|
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK DYNJ38587A, DYNJ38587B BIOPSY/DRAINAGE TRAY-LF DYNJ30078D W LINQ PACK DYNJ59108B
Unapproved design changes to the products outside of the 510(k) clearance.
|
FDA
Z-1879-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
|
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes MINOR ENT SINUS PACK-LF DYNJ0101278F DYNJ0101278G DYNJ0101278I SINUS PACK DYNJ56262
Unapproved design changes to the products outside of the 510(k) clearance.
|
FDA
Z-1880-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
|
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 15mm-16.5mm-18mm, REF 1205-18
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
|
FDA
Z-1940-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 18, 2026
|
Details |
|
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
|
FDA
Z-1905-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 25, 2026
|
Details |
|
Medline Kits: 1) GYN LAPAROSCOPY PACK, Model Number: DYNJ41257F
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1846-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Medline Syringes: 1) SYRINGE 12ML CONTROL W/ROTATOR, Model Number: DYNJSYR12CWR; 2) SYRINGE 10ML CONTROL W/ROTATOR, Model Number: DYNJSYR10CWR; 3) SYR CONTROL PAD 12ML L/L, Model Number: DYNJSYR12CP; 4) TBG PRESS 72IN M/F ROT BRAID, Model Number: DYNJBRT72R; 5) SYRINGE 10ML CONTROL MLL, Model Number: DYNJSYR10C; 6) SYRINGE 8ML CONTROL MLL, Model Number: DYNJSYR8C; 7) SYRINGE 12ML CONTROL MLL, Model Number: DYNJSYR12C; 8) SYR CONTROL PAD 10ML L/L ROT, Model Number: DYNJSYR10CRP; 9) SYR CONTROL PAD 12ML L/L ROT, Model Number: DYNJSYR12CRP; 10) CTRL SYRINGE 6ML RING ROT L/L, Model Number: DYNJSYR
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1831-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Medline Kits: 1) NEWBORN ADMISSION, Model Number: DYKB1038; 2) DRAINAGE TRAY, Model Number: DYNDA3188; 3) VA ORLANDO SHOULDER PACK, Model Number: DYNJG001027B; 4) TUMESCENT SYRINGE KIT, Model Number: DYNJTUMSYR; 5) OMC PTCA PACK, Model Number: DYNJT3719; 6) PORT PACK, Model Number: DYNJT5667; 7) WASTE MANAGEMENT KIT - 2, Model Number: DYNJWASTEKIT2; 8) CARDIAC CATH, Model Number: DYNJ20175J; 9) D&C PACK-POB, Model Number: DYNJ33521D; 10) BASIC PACK, Model Number: DYNJ38533F; 11) CATH PACK IMPLANT, Model Number: DYNJ39230D; 12) CERVICAL SPINE PACK, Model Number: DYNJ40886B; 13) MV-IR ANGIO DRAP
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1842-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
|
FDA
Z-1900-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 25, 2026
|
Details |
|
Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF, Model Number: DYNJ32841F; 2) CRANIOTOMY PACK-LF, Model Number: DYNJ46069D 3) CAMPUS EXTREMITY PK, Model Number: DYNJ51935A 4) FOOT -XRAY BOWL MEDCUP SPECCUP, Model Number: DYNJ68902A 5) RADIOLOGY SPINE PACK, Model Number: DYNJ80679A 6) DR CHA CUSTOM PACK, Model Number: DYNJ82370A 7) SPINE PACK HC, Model Number: DYNJ84272
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1849-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 35cm. Model Number: TB2-0535FC.
Potential for detachment of a distal tip component of the device during use.
|
FDA
Z-1853-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 23, 2026
|
Details |
Recent Product Recall Alerts
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-Risk Recall Updates
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
Daily Official Source Coverage
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
Latest Recalls By Source Agency
Use the source notes to understand which agency published the notice and what type of product it covers.
Latest Consumer Product Recalls
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
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Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
Latest Meat And Poultry Recall Alerts
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
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New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
How To Use The Latest Product Recalls Page
Check The Publish Date First
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
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Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Prioritize High-Risk Notices
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Verify The Official Notice
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
Latest Product Recalls FAQ
Helpful context for searches such as product recalls today, recent product recalls and recall alerts.
How often is the latest product recall list updated?
The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
Why do some recent recalls have older recall dates?
Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.
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Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
Can I get only high-risk recalls?
Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.