Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 526 - 550 of 3,083 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Plum Duo Infusion Pump, 40002-0401 Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.	FDA Z-2312-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 29, 2026	Details
CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040 Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.	FDA Z-2330-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
Halyard, Eye Bag Pack. Kit Code: UIEB48-01. Inadvertent distribution of sealed pouches that had not undergone validated sterilization.	FDA Z-2410-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Hintermann Series Talar Implant, Left, Size 2 REF 302112 Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.	FDA Z-2399-2026	Medical Device	High	Jun 17, 2026 Recall: Mar 24, 2026	Details
Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure. Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.	FDA Z-2413-2026	Medical Device	High	Jun 17, 2026 Recall: May 12, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2341-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.	FDA Z-2354-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2351-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G; Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-lock leaks during manipulation of the frangible and tubing when preparing the product for use for treatment. This issue presents the potential of a slip and fall hazard associated with fluid on the floor.	FDA Z-2321-2026	Medical Device	High	Jun 17, 2026 Recall: May 12, 2026	Details
Halyard, Drape Pack. Kit Code: LMDP36-01. Inadvertent distribution of sealed pouches that had not undergone validated sterilization.	FDA Z-2409-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2345-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2350-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2340-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Plum Duo Precision IV Pump, 40002-0403 Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.	FDA Z-2313-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 29, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2342-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2333-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2336-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Model/Catalog Number: 1023770 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 12 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, C Due to incorrect incubation process being performed on product.	FDA Z-2332-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 13, 2026	Details
Allia IGS 5 Pulse angiographic X-ray system GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.	FDA Z-2315-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 20, 2026	Details
Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge.	FDA Z-2398-2026	Medical Device	High	Jun 17, 2026 Recall: May 7, 2026	Details
CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930 Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.	FDA Z-2327-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in) REF:TCN-15, TCN Electrode, NITINOL, 15 cm x 0.45 mm (0.0175 in); REF:TCN-20, TCN Electrode, NITINOL, 20 cm x 0.45 mm (0.0175 in) REF: TCN-5-3m, TCN Electrode, NITINOL, 3M CABLE, 5 cm x 0.45 mm (0.0175 in) REF: TCN-10-3M, TCN Electrode, NITINOL, 3M CABLE, 10 cm x 0.45 mm (0.0175 in); REF: TCN-15-3M, TCN Electrode, NITINOL, 3M CABLE, 15 cm x 0.45 mm (0.0175 in) REF: TCN-20-3M, TCN Electrode, NITINOL, 3M CABLE, 20 cm x 0.45 mm (0.0175 in Reusable electrodes may not meet expected performance levels.	FDA Z-2403-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 29, 2026	Details
MOSAIQ Oncology Information System Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.	FDA Z-2406-2026	Medical Device	High	Jun 17, 2026 Recall: May 21, 2026	Details
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, C Due to incorrect incubation process being performed on product.	FDA Z-2331-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 13, 2026	Details
Allia Moveo angiographic X-ray system GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.	FDA Z-2318-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 20, 2026	Details

Showing 526 - 550 of 3,083 product recalls

Prev 1 ... 20 21 22 23 24 ... 124 Next

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

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.

CPSC

Latest Consumer Product Recalls

New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.

FDA

Latest Food And Medical Device Recalls

Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.

USDA FSIS

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.

NHTSA

Latest Vehicle Recall Campaigns

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.

Filter By Product Type

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.

What should I check on a recent food recall?

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.

Find Recent Product Recall Alerts