Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 151 - 175 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Jovy Gummy Worms Neon; packaged in 1lb plastic units. UPC 712199083411 undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1)	FDA H-0130-2027	Food	High	Oct 28, 2026 Recall: Aug 24, 2026	Details
Direxion Torqueable Microcatheter, NGMC/FATHOM/027/STRAIGHT/1RO/130; Material Number: M001195710 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0255-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
VOCSN+Pro, Model Number:PRT-00490-001, Package PN:PRT-00853-000. used for ventilatory support. Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.	FDA Z-0122-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 17, 2026	Details
MEDLINE DRAPE C-SECTION W/POUCH ST 7/CS, Medline Product Number/SKU DYNJP6101 Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.	FDA Z-0269-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 9, 2026	Details
Techno-Path Multichem AE Unassayed Level 3, REF:AE623X A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material. Additional testing confirmed that the labelled shelf-life performance claim for the Ammonia analyte can no longer be supported for the affected lots. This issue is limited to the Ammonia analyte only. The impacted device may cause delay of issuing results to the physician. Delayed recognition and diagnosis of elevated levels may impact in timely treatment of life-threatening levels described within medical toxicity intervention decision points.	FDA Z-0207-2027	Medical Device	High	Oct 28, 2026 Recall: Aug 14, 2026	Details
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/1RO/130; Material Number: M001195210 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0224-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
VC+Pro Model Number: PRT-00900-001, Package PN:PRT-00973-000. used for ventilatory support. Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.	FDA Z-0124-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 17, 2026	Details
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/2RO/155; Material Number: M001195330 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0236-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF, Medline Kit Number/SKU DYNJ16127N; 2) NYGH-DELIVERY PACK-LF, Medline Kit Number/SKU DYNJ27206D; 3) OB/GYN, Medline Kit Number/SKU DYNJ911652. Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.	FDA Z-0276-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 9, 2026	Details
V*Home, Model Number: PRT-01444-000, Package PN:PRT-01445-000. used for ventilatory support. Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.	FDA Z-0133-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 17, 2026	Details
V+Pro Model Number: PRT-01185-000, Package PN:PRT-01198-000; Model Number: PRT-01185-001, Package PN: N/A; Model Number: PRT-01185-002, Package PN:N/A. used for ventilatory support. Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.	FDA Z-0129-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 17, 2026	Details
InterStim SureScan MRI Leads 978A1 & 978B1: LEAD 978A128 ISTM MICRO 28CM SSMRI TINED 978A128 LEAD 978A133 ISTM MICRO 33CM SSMRI TINED 978A133 LEAD 978A141 ISTM MICRO 41CM SSMRI TINED 978A141 LEAD 978B128 ISTM II 28CM SSMRI TINED 978B128 LEAD 978B133 ISTM II 33CM SSMRI TINED 978B133 LEAD 978B141 ISTM II 41CM SSMRI TINED 978B141 Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may result in delay of surgery or need for surgical replacement of the product.	FDA Z-0266-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 8, 2026	Details
Xact mole marker for mammography Model/Catalog Number: M15RM The radiopaque material may detach from the marker. In some cases, artifact was noted and attributed to the detached material.	FDA Z-0268-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 22, 2026	Details
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/2RO/130; Material Number: M001195320 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0235-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/J/1RO/130; Material Number: M001195270 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0230-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
MEDLINE medical convenience kits labeled as: 1) FETAL SURGERY CDS-LF, Medline Kit Number/SKUCDS840214R; 2) MAJOR, Medline Kit Number/SKUDYNJ904851I; 3) ABDOMINAL TRANSPLANT, Medline Kit Number/SKUDYNJ908124B. Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.	FDA Z-0274-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 9, 2026	Details
Generic Name: restor3d MTP Implant Generic Name: MTP Implant Model/Catalog Number: 1103-161620 Software Version: None Product Description: The restor3d Metatarsophalangeal (MTP) Implant is a sterile, single-use implant grade metal device, available in varied articulating surface coverages. The restor3d MTP implant is designed to replace the damaged articulating surface of the first metatarsal distal head. The device is intended for the treatment of patients with degenerative and post-traumatic arthritis in the first metatarsal joint in the presence of good bone stock and integrity of the first Implants were found in the field with orange sterilzation indicators which means implants were not exposed to sterilization.	FDA Z-0264-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 4, 2026	Details
Generic Name: Softmed Breathables Advanced Toric (fanfilcon A) Soft (Hydrophilic) Contact Lens; Model/Catalog Number: Softmed Breathables Advanced Toric Product Description: 55% water content, toric, silicone hydrogel contact lens for daily wear, frequent replacement. Blister packaged. The affected products bear an incorrect statement on the carton packaging indicating that the product is "Indicated for Extended Wear". However, this product is intended for daily wear, and the extended-wear statement should not have appeared on the affected carton labeling. This product is not approved by the U.S. Food and Drug Administration (FDA) for extended wear use.	FDA Z-0204-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 22, 2026	Details
MEDLINE DRAPE C-SECTION FEN CLR SCREEN W, Medline Product Number/SKU DYNJP6108 Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.	FDA Z-0271-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 9, 2026	Details
Direxion Torqueable Microcatheter, NGMC/FATHOM/021/BERN/1RO/155; Material Number: M001195650 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0252-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
Direxion Torqueable Microcatheter, NGMC/TRANSEND/021/BERN/1RO/155; Material Number: M001195850 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0261-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
Direxion Torqueable Microcatheter, NGMC/SINGLE/027/J/1RO/155; Material Number: M001195480 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0246-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
MEDLINE medical convenience kits labeled as: C-SECTION PACK, Medline Product Number/SKU DYNJ48455A Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.	FDA Z-0273-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 9, 2026	Details
Direxion Torqueable Microcatheter, NGMC/FATHOM/021/BERN/1RO/130; Material Number: M001195640 The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.	FDA Z-0251-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 16, 2026	Details
MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD, Medline Product Number/SKU DYNJ906291G Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.	FDA Z-0279-2027	Medical Device	High	Oct 28, 2026 Recall: Sep 9, 2026	Details

Showing 151 - 175 of 4,622 product recalls

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