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 1,551 - 1,575 of 3,321 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Catalog No.: 10714040; Product/UPN No.: H787107140405 (Box), H787107140400 (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-1868-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute 90-300-251008: nanOss 3D Advanced Bone Graft Substitute, 25x100x8mm, 20cc 90-300-25508: nanOss 3D Advanced Bone Graft Substitute, 25x50x8mm, 10cc 90-300-251004: nanOss 3D Advanced Bone Graft Substitute, 25x100x4mm, 10cc 90-400-25508: nanOss 3D Plus Advanced Bone Graft Substitute, 25x50x8mm, 10cc
Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
|
FDA
Z-1897-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 9, 2026
|
Details |
|
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;
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-1857-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No.: 10714011; Product/UPN No.: H787107140115 (Box), H787107140110 (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-1861-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O serotype as a 2-O serotype.
|
FDA
Z-1923-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 25, 2026
|
Details |
|
Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT, Model Number: DYNJ24517D
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
|
FDA
Z-1832-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 25, 2026
|
Details |
|
Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)
Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants
|
FDA
Z-1927-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 20, 2026
|
Details |
|
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ARTERIOGRAM TRAY 00-402001T, 00-402001U CATH LAB-VEIN PROCEDURES DYNJ60329A CENTRAL VENOUS ACCESS PACK-LF CVI5070 FISTULAGRAM PACK DYNJ66259 INVASIVE LINE INSERTION DYNJ44123C NON VASCULAR PACK DYNJ68037B, DYNJ68037C PICC ABSCESS PACK-LF DYNJ0774005G PICC LINEPACK (PCLUI)642-LF DYNJ47717B PICC PHC DYNJ37484C
Unapproved design changes to the products outside of the 510(k) clearance.
|
FDA
Z-1891-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Feb 27, 2026
|
Details |
|
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen Central Venous Access Device with Arrowg+ard Blue technology permits short-term (<30 days) venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins. The Arrowg+ard technology is intended to help provide protection against catheterrelated infections. Clinical data have not been collected that demonstrate the use of the Arrowg+ar
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
|
FDA
Z-1917-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 11, 2026
|
Details |
|
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14433
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
|
FDA
Z-1919-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 11, 2026
|
Details |
|
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116.
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
|
FDA
Z-1904-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 25, 2026
|
Details |
|
Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is intended for injection or aspiration of fluids. The needle protection device covers the needle after use to help prevent needle sticks.
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
|
FDA
Z-1910-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 11, 2026
|
Details |
|
AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box), H787137097040 (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-1874-2026
|
Medical Device | High |
Apr 29, 2026
Recall: Mar 3, 2026
|
Details |
|
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 |
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
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Latest Recalls By Source Agency
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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.
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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.
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Check The Publish Date First
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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
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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.
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Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.