Colorado recalls

Certain lots of Medtronic DLP Retrograde Cannula (Model 94725), a catheter used in heart surgery, may have a breach in their sterile packaging. This could potentially expose the device to contamination before use. The affected lots have been identified by lot number and GTIN code.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94665) used in heart-lung bypass surgery may have a compromised sterile barrier. This could allow contamination of the device before use. The affected lots have been identified and distributed worldwide.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94215T), a catheter used during heart surgery, may have a compromised sterile barrier. This affects 600 units distributed worldwide. No injuries have been reported.

Certain lots of Medtronic GUNDRY Retrograde Cannula (Model 94115T), a catheter used during heart-lung bypass surgery, may have a breach in their sterile packaging. This could allow contamination of the device before use. The affected lots have been identified and are listed in the recall notice.

Certain lots of Medtronic GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, may have a breach in the sterile barrier. This could allow contamination of the sterile product before use during heart surgery.

The straight inserter tool on certain OneLIF Interbody Cage implants may fail to attach properly to the cage. This could prevent secure engagement during spinal fusion surgery, potentially causing procedural delays or requiring surgeons to choose a different implant.

ICU Medical oncology infusion kits with extension sets may develop leaks during chemotherapy administration. If a leak occurs during therapy, patients may receive less medication than intended, and healthcare workers or patients could be exposed to hazardous drugs.

Tangent Endoscopy's Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) can develop fractures at the tip of the shaft during use. While the fractured pieces have not completely detached in reported cases, a broken catheter tip could affect device function or potentially cause patient harm.

Certain Swan-Ganz Pacing Catheters (Model D200F7) may leak or break at the blue proximal injectate lumen hub due to manufacturing and material changes. This can result in infection, medication loss, or blood loss during use.

Certain Swan-Ganz Jr Catheter models may leak or break at the blue proximal injectate lumen hub due to manufacturing and material changes. This can result in infection, loss of medication, or blood loss during use.

Certain Swan-Ganz catheters may leak or break at the blue proximal injectate lumen hub due to manufacturing and material changes. This defect can result in loss of medication, blood loss, or infection during use.

John B Sanfilippo & Sons recalled Fisher Tex Mex Trail Mix (30 oz jars, UPC 070690275941) because it may contain Salmonella. The affected product has a "Best By" date of 08/06/27. About 606 cases were distributed nationwide.

Good & Gather Mexican Street Corn Trail Mix (8 oz bags, UPC 085239270240) may contain Salmonella. The affected products have a "Best By" date of March 23, 2027. No illnesses have been reported so far.

Squirrel Brand Town & Country Mix nuts and seeds in 16 oz and 7.5 oz cans may contain Salmonella. The recall affects products with best-by dates of 05/01/27, 05/25/27, 05/28/27, and 02/10/27 distributed nationwide.

Squirrel Brand Travelers Mix 16 oz cans may contain Salmonella, a harmful bacteria that can cause serious illness. The recall affects cans with best-by dates of 04/30/27, 05/28/27, or 06/24/27, distributed nationwide.

John B Sanfilippo & Sons is recalling Southern Style Nuts Hunter Mix (30 oz jars) because some packages may contain Salmonella. The affected product was distributed nationwide. No illnesses have been reported so far.

Southern Style Nuts Gourmet Hunter Mix in 23 oz and 36 oz jars may contain Salmonella. The affected products have best-by dates ranging from January 28, 2027 through April 2, 2027. No illnesses have been reported.

PS Seasoning & Spices non-fat dry milk was made with milk powder that a supplier recalled due to Salmonella contamination. The affected product is 1 lb packages with lot number 2025-45065 and expiration date 06/06/2027. About 264 lbs were distributed nationwide.

PS Seasoning & Spices produced a food binding product using milk powder that was contaminated with Salmonella. The contamination was identified by the milk powder supplier and led to this recall. The affected product is a 50-pound commercial ingredient sold under the Save A Lot Bind name.

Blackstone Parmesan Ranch Seasoning was made with milk powder that a supplier recalled due to Salmonella contamination. The affected seasoning was distributed nationwide. No illnesses have been reported.

PS Seasoning & Spices recalled a jalapeno heat unit seasoning (Part #180002945, 18 lbs) because it was made with milk powder that a supplier recalled due to Salmonella contamination. The affected product has lot #2025-44769 with expiration date 05/27/2027.

PS Seasoning & Spices' 1P Original Smokehouse Unit seasoning mix (Part #180002964, Lot #2025-44770) was made with milk powder that a supplier recalled due to Salmonella contamination. The affected product is a 15.10 lb bulk seasoning designed for smoking meat.

PS Seasoning & Spices recalled Ellsworth Sour Cream + Onion Seasoning because it was made with milk powder that was contaminated with Salmonella. The affected product is a bulk seasoning (25-lb bags) distributed nationwide. Lot #2026-51127 is included in this recall.

Llorens Pharmaceuticals is recalling Vitamin B-Complex, Vitamin C & Folic Acid dietary supplement (8 FL Oz bottles, Lot B2025, expiration 08/27) because some bottles contain black particulate matter. The contamination was identified before causing reported injuries.

Wellnov Supplements LLC's Liposomal Sleep Spray was manufactured without proper safety controls, creating the potential for bacterial contamination and botulism. The affected product was distributed nationwide and in Puerto Rico between October 2025 and April 2026.

Wellnov Liposomal B12 Spray was manufactured with deviations from safety standards that could allow bacterial pathogens, including botulism-causing bacteria, to contaminate the product. The affected bottles were distributed nationwide and to Puerto Rico between October 2024 and April 2026.

Wellnov Supplements LLC is recalling Liposomal D3+B12 Spray due to manufacturing process deviations that could allow bacterial pathogens, including C. botulinum, to contaminate the product. The affected spray (lot DB1024, expiration 10/2026) was distributed nationwide and in Puerto Rico between October 2024 and April 2026.

Wellnov Supplements LLC recalled its Liposomal D3-5000IU Spray due to manufacturing process deviations that could allow bacterial contamination, including potential botulism-causing bacteria. The affected product is a 30 ml aluminum bottle spray (lot DS1024, expiration 10/2026) distributed nationwide between October 2024 and April 2026.

Wellnov Supplements LLC is recalling Liposomal Prenatal+Postnatal Liquid Multivitamin Drops (Iron Free) due to manufacturing deviations that could allow bacterial pathogens, including C. botulinum, to contaminate the product. The affected bottles were distributed nationwide between September 2024 and April 2026.

Wellnov Supplements LLC is recalling Liposomal Women's Liquid Multivitamin Drops (Iron Free) due to manufacturing issues that could allow bacterial growth, including a potential risk of botulism. The product was distributed nationwide and in Puerto Rico between October 2024 and April 2026.