Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 2,251 - 2,275 of 3,085 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Campy CVA Medium 100/PK, R01272 Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.	FDA Z-1474-2026	Medical Device	High	Mar 4, 2026 Recall: Feb 5, 2026	Details
Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1441-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1453-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1457-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
PIE PAK Models: P2HC-A, P2HC-S, P2HC Lack of 510K clearance	FDA Z-1462-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 14, 2026	Details
Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1440-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MJSALINE7 Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.	FDA Z-1435-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 5, 2026	Details
Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1449-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR Software anomaly in the patient positioning system may result in positional discrepancy.	FDA Z-1429-2026	Medical Device	High	Mar 4, 2026 Recall: Feb 6, 2026	Details
Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1452-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036 Knee and Humeral socket implants contain incorrect labeling.	FDA Z-1460-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 15, 2026	Details
Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1448-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU EBSI1498 Medline DIALYSIS DRESSING CHANGE KIT SKU EBSI1107 EBSI1596 EBSI1781 EBSI1812 Centurion DIALYSIS/PHERESUS CVC DRSG CHANGE KIT SKU DT22630 Medline DIALYSIS/PHERESIS DRESSING CHANGE KIT SKU EBSI1470 Centurion VASCATH DRESSING CHANGE TRAY SKU DT22845 Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.	FDA Z-1467-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200 Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.	FDA Z-1463-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528 Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.	FDA Z-1434-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 5, 2026	Details
Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1444-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1 During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.	FDA Z-1473-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 13, 2026	Details
Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1439-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1447-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1446-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1455-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1445-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Convenience kits used for dialysis maintenance Medline ADD A CATH DIALYSIS KIT SKU ECVC8415A Centurion CENTRAL LINE INSERTION TRAY SKU DT19810 Centurion DIALYSIS BUNDLE WITH NO CATHETTER SKU CVI4310A Medline DIALYSIS CAP CHANGE KIT SKU DYNDC2425 Medline DIALYSIS CHANGE KIT SKU EBSI1453A Centurion HEMODIALYSIS ACCESS KIT SKU DT12970 Medline LARGE BORE, DIALYSIS, ENHANCED SECUREMENT SKU EBSI1741 Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.	FDA Z-1465-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1450-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with SL-110, Mobile Exam Light Due to battery component overheating while charging resulting in melting of internal components and causing smoke.	FDA Z-1436-2026	Medical Device	High	Mar 4, 2026 Recall: Oct 13, 2025	Details

Showing 2,251 - 2,275 of 3,085 product recalls

Prev 1 ... 89 90 91 92 93 ... 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