Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 2,426 - 2,450 of 3,321 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
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
Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1442-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Model/Catalog Number: 509-00-432 Knee and Humeral socket implants contain incorrect labeling.	FDA Z-1458-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 15, 2026	Details
Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1454-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167 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-1468-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746 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-1464-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER FISH); DISTRIBUTED BY: PFP LLC, Brooklyn, NY, 11211, USA; Product must be thoroughly cleaned and cooked before consumption.; PRODUCT OF VIETNAM; UPC: 6 946976 818000 Uneviscerated Fish	FDA H-0519-2026	Food	High	Mar 4, 2026 Recall: Feb 3, 2026	Details
Mung Beans packaged in 4lb polybags; 6-4lb bags per carton Presence of Thiamethoxam-PESTICIDE	FDA H-0524-2026	Food	High	Mar 4, 2026 Recall: Jan 15, 2026	Details
Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug with plastic caps: 1. 1 Gal Net 128 Fl oz. UPC 0 31193-00701 9. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. 2. 2.5 Gallon Net (320 Fl oz./9.4L). UPC 0 31193-01501 4. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. 3. Infant Water, 1 Gal Net, 128 FL. Oz. Not sterile. Use as directed by physician or by labeling directions for use of infant formula. UPC 0 31193-01401 7. 4. Daisy's Doggy Water, 1 Gal Net, 128 FL. Oz. 100% Pure Water. No Chlorine. UPC 0 31193-90100 3. Bottled by Water was bottled under insanitary conditions.	FDA H-0534-2026	Food	High	Mar 4, 2026 Recall: Feb 6, 2026	Details
IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corrugated 30lbs. case or packaged in polyethylene liner within a Gaylord 1400lbs. tote. Product was not sold to consumers from retail stores. Willamette Valley Fruit Company 2994 82nd Ave. NE Salem OR 97305 Listeria monocytogenes	FDA H-0522-2026	Food	High	Mar 4, 2026 Recall: Feb 12, 2026	Details
Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case The products contain an unallowed color Carmoisine (E122) - Acid Red 14.	FDA H-0527-2026	Food	High	Mar 4, 2026 Recall: Nov 21, 2025	Details
Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged in a plastic resealable bag with UPC 015000005962, packed 4 bags/case with UPC 015000935726; Made for Gerber Products Co., Fremont, MI 49413 Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.	FDA H-0518-2026	Food	High	Mar 4, 2026 Recall: Jan 26, 2026	Details
Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case The products contain an unallowed color Carmoisine (E122) - Acid Red 14.	FDA H-0528-2026	Food	High	Mar 4, 2026 Recall: Nov 21, 2025	Details
Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label is read in parts: *INGREDIENTS: SugarWhey Powder, Nonfat Milk Powder, Soy LecithinPeanut Butter (peanuts, peanut oil), Pretzels (wheat flourbuttermilk solidsCONTAINS MILK AND SOY May contain wheat, peanuts and tree nuts*" Ingredients List declares peanut but the Contains statement does not declare peanut	FDA H-0523-2026	Food	High	Mar 4, 2026 Recall: Jan 30, 2026	Details
Valley Springs Steamed Distilled Water. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-00601 2. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901. Water was bottled under insanitary conditions.	FDA H-0536-2026	Food	High	Mar 4, 2026 Recall: Feb 6, 2026	Details
Yoyo Gummy Grape Plus Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case The products contain an unallowed color Carmoisine (E122) - Acid Red 14.	FDA H-0529-2026	Food	High	Mar 4, 2026 Recall: Nov 21, 2025	Details

Showing 2,426 - 2,450 of 3,321 product recalls

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