Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 1,801 - 1,825 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470033, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only). Potential Salmonella contamination	FDA H-1100-2026	Food	High	Jul 1, 2026 Recall: Jan 9, 2026	Details
Joy Saffron Cardamon Lassi 16 oz. Product not adequately pasteurized	FDA H-1094-2026	Food	High	Jul 1, 2026 Recall: Apr 23, 2026	Details
Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.43 oz. (1 lb. 6.4 oz.) 636g UPC 8 70375 00511 1; 6 retail units per case Motor City Pizza Co. 5 Cheese Bread Twin retail pack; 44.86 oz. (2 lb. 12.9 oz.) 1272g UPC 8 70375 00509 8; 10 retail units per case potential salmonella contamination	FDA H-1095-2026	Food	High	Jul 1, 2026 Recall: May 29, 2026	Details
1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag. Potential presence of Salmonella.	FDA H-1112-2026	Food	High	Jul 1, 2026 Recall: Apr 28, 2026	Details
2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag. Potential presence of Salmonella.	FDA H-1117-2026	Food	High	Jul 1, 2026 Recall: Apr 28, 2026	Details
boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 LB) 750g Ingredients: Organic wheat flour ... Contains Wheat Topped flavors may additionally contain ... sesame seeds ... Best by SE 26 26 UPC: 850016588067 Undeclared allergen, sesame.	FDA H-1133-2026	Food	High	Jul 1, 2026 Recall: May 22, 2026	Details
1.5oz, 2oz Dirty Brand Salt and Vinegar Potato Chips , Plastic Bag. Potential presence of Salmonella.	FDA H-1114-2026	Food	High	Jul 1, 2026 Recall: Apr 28, 2026	Details
Dried Herring Fish 7 oz. Improperly eviscerated which may result in Clostridium botulinum contamination	FDA H-1080-2026	Food	High	Jul 1, 2026 Recall: Jun 2, 2026	Details
Joy Pineapple Lassi 16 oz. Product not adequately pasteurized	FDA H-1085-2026	Food	High	Jul 1, 2026 Recall: Apr 23, 2026	Details
Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.H1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2566-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Octopus 4 Tissue Stabilizer, Model 29400 During the manufacturing process, 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-2577-2026	Medical Device	High	Jul 1, 2026 Recall: May 12, 2026	Details
Da Vinci ASSY, PSS, SP1098, Part Number: 380601 Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs out it may cause restricted column range of motion and/or uncontrolled motion, which may cause patient tissue injury/crushing injury/bleeding.	FDA Z-2521-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 22, 2026	Details
INZONE DETACHMENT SYSTEM, REF: M00345100950 Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be unable to detach a coil as intended, which may necessitate medical intervention if the procedure must be completed with an alternative technique.	FDA Z-2552-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 6, 2026	Details
Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2565-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435. Potential for thrombus formation during prolonged use of the introducer.	FDA Z-2600-2026	Medical Device	High	Jul 1, 2026 Recall: May 22, 2026	Details
Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476 Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.	FDA Z-2531-2026	Medical Device	High	Jul 1, 2026 Recall: May 20, 2026	Details
Octopus Evolution AS Tissue Stabilizer, Model TS2500 During the manufacturing process, 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-2576-2026	Medical Device	High	Jul 1, 2026 Recall: May 12, 2026	Details
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2572-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2561-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.	FDA Z-2522-2026	Medical Device	High	Jul 1, 2026 Recall: May 26, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CRANIOTOMY PACK-LF DYNJ0101292F DYNJ0101292G HYBRID PACK DYNJ65925A LAMINECTOMY DYNJ905156L DYNJ905156M DYNJ905156N DYNJ905156O DYNJ905156P MAJOR EXTREMITY DYNJ905159F DYNJ905159I DYNJ905159J DYNJ905159K NEURO CERVICAL PACK DYNJ0101287J DYNJ0101287K NEURO SPINE PACK DYNJ81612C POSTERIOR SPINE PACK-LF DYNJ0843339L DYNJ0843339M DYNJ0843339N SPINE PACK DYNJ30150F Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.	FDA Z-2587-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2562-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834. Potential for thrombus formation during prolonged use of the introducer.	FDA Z-2601-2026	Medical Device	High	Jul 1, 2026 Recall: May 22, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO PACK DYNJ30565C DYNJ32555B ANGIO PACK-LF DYNJ0774765U ANGIO TRAY DYNJ46153A ANGIOGRAM TRAY DYNJ33638K ANGIOGRAPHY DRAPE PK QVH-LF DYNJ35110D ANGIOGRAPHY PACK DYNJ44293D ANGIOGRAPHY PACK-LF DYNJ0854485T DYNJ35916J GENERAL ANGIO PACK DYNJ57760B GENERAL ENDO PACK-LF DYNJ0842873J JUDKINS PACK DYNJ51126A RADIOLOGY ANGIO MAJOR PACK DYNJ62858B TAVR JUDKINS PACK DYNJ51127B Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.	FDA Z-2591-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR VASCULAR PACK DYNJ81610C MINIMALLY INVASIVE PACK-LF DYNJ0843063L PEDIATRIC CATH ANGIO PACK DYNJ54755J PERIPHERAL ARTERIOGRAM RAD DYNJ61383C POSTERIOR SPINE PACK-LF DYNJ0843339O UPPER EXTREMITY DYNJ61907A VISCERAL ANGIOGRAM PACK-LF DYNJ0429121L Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.	FDA Z-2590-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details

Showing 1,801 - 1,825 of 4,622 product recalls

Prev 1 ... 71 72 73 74 75 ... 185 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