Louisiana recalls

Mobius Imaging recalled certain replacement pendant components for AIRO CT X-ray systems because they are missing a required "Safe Hand Position Warning" label. The label is important safety information for users of the equipment. No injuries have been reported.

The handle on the orthopedic rotation tool in Medicrea's IB3D PL Instruments Set may become detached from the shaft during surgery, preventing proper rotation of the implant. This affects 44 units distributed across multiple U.S. states. No injuries have been reported.

Medicrea's IB3D Universal Implant Inserter tool handle may separate from the shaft during surgery, preventing the surgeon from rotating the implant as intended. The issue affects 44 units across multiple states. No injuries have been reported.

Repligen is recalling the MAVERICK Measurement Module Spectrometer due to cable connection defects that can cause two problems: the laser output may increase to unsafe levels, or the laser may fire unexpectedly during normal operation. A loose or poorly crimped cable under stress can trigger these faults. No injuries have been reported.

Abbott Diabetes Care is recalling certain FreeStyle Libre 3 Plus continuous glucose monitoring sensors due to a manufacturing issue that may cause carbon buildup inside the sensor. This buildup could lead to incorrect low blood sugar readings, which may not alert you when your glucose is actually low.

Abbott has recalled certain FreeStyle Libre 3 Plus glucose sensors due to a manufacturing issue that may cause carbon buildup inside the sensor. This buildup can result in the sensor showing incorrect low blood sugar readings when your actual glucose is normal or higher. The recall affects specific lot numbers with expiration date of 01/31/2026.

Abbott has recalled certain FreeStyle Libre 3 Plus glucose sensors due to a manufacturing issue that may cause carbon buildup inside the sensor. This buildup could result in the sensor showing incorrect low blood sugar readings when your actual glucose is normal or high.

Abbott is recalling certain FreeStyle Libre 3 sensors due to a manufacturing defect that may cause carbon buildup inside the sensor. This buildup can result in the sensor showing incorrect low blood sugar readings when your actual glucose level is normal or higher. The recall affects sensors with specific lot and serial numbers expiring by December 31, 2025.

Ice can form in the venting system of Canon Medical VANTAGE TITAN 3T MRI machines (models MRT-3010/MEXL-3010). If the system undergoes a quench event while ice is present, helium gas may not escape properly and pressure inside the helium vessel could build up and rupture, releasing helium gas into the scanning room.

There is a potential for formation of ice occurring in the venting system of the superconducting magnet of the MRI systems. if a quench occurs in this condition, helium gas may not be able to escape via the designed vent paths, and the pressure in the helium vessel may rise. This pressure build-up could eventually rupture the helium vessel, causing helium gas to be released into the MR scanning room.

Herbs Forever's Hingwastika Churna Ayurvedic supplement contains wheat that is not listed on the label. This poses a serious risk to people with wheat allergies or celiac disease. The affected batch is 622-2 with an expiration date of 6/2029.

Herbs Forever Gastro Care Ayurvedic herbal supplement capsules may contain wheat that is not listed on the label. This poses a serious risk to people with wheat allergies or celiac disease. The affected batch is 124-4 with expiration date 1/2029.

AZ Gems Jumbo Raw Shrimp (2 lb bags, UPC 1 93968 00697 6) contains elevated levels of chloramphenicol, an antibiotic not approved for use in the U.S. food supply. The affected product was distributed nationwide under the Member's Mark label. No illnesses have been reported to date.

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk non-dairy frozen dessert may contain foreign material. The recall affects specific batches distributed across the US and Canada. No injuries have been reported.

Sanders Candy Factory Inc. is recalling frosted almonds (bulk product code 23208, lot codes 058.25 and 070.25) due to elevated levels of aflatoxin, a naturally occurring toxin that can cause serious health problems. The affected product was identified before it reached consumers and was only distributed to a commercial customer.

Cipla USA is recalling certain pre-filled syringes of Lanreotide Injection 120 mg because they may contain particulate matter (small particles) in the solution. The affected syringes have specific lot numbers and expiration dates between October 2026 and March 2027. No injuries have been reported so far.

Several Colgate and Crest toothpaste products distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure and activity. The FDA found insanitary conditions at the distribution center that do not meet manufacturing standards. No injuries have been reported.

Gold Star Distribution Inc. distributed multiple Axe body sprays and Lucky deodorant products that were stored in conditions with rodent activity. The FDA found insanitary handling at their distribution center. No injuries have been reported.

Gold Star Distribution Inc. distributed several petroleum jelly products that were stored in insanitary conditions, including exposure to rodents, at their distribution center. The affected products include Vaseline, Lucky, Personal Care, and Softee petroleum jelly in various sizes and formulations. All lots distributed by Gold Star that have not expired may be affected.

Lucky Ice Cool Mouthwash was distributed from a facility with insanitary conditions, including rodent exposure and activity. The FDA is recalling all unexpired lots of this product due to potential contamination from the distribution center conditions.

Gold Star Distribution's 4 oz vaporizing chest rub was distributed from a facility with insanitary conditions, including rodent exposure. The product may have been contaminated during storage or handling at their distribution center.

Carmex lip balm products distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure and activity. The products may have been affected by insanitary conditions at their distribution center. This recall affects jars and tubes sold nationwide.

Gold Star Distribution's 8oz ice gel products were stored in conditions where rodents were present in their distribution center. The FDA found insanitary conditions that do not meet required manufacturing and distribution standards. All unexpired lots distributed by this company are affected.

Swan White Clear Alcohol (50%, 16oz bottles) distributed by Gold Star Distribution Inc. was stored in conditions with rodent exposure and activity, along with other sanitation violations. This affected all lots still within expiration across the U.S.

TUMS antacid tablets distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure at their distribution center. This applies to TUMS Assorted 12-count, Extra Strength Assorted Berries 12-count (#1194A, dated 05/27), and Extra Strength Assorted Fruit 12-count (#1194C, dated 03/27) sold nationwide. No injuries have been reported.

Halls Cough Drops distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure and activity at their distribution center. This creates a potential contamination risk. The recall affects multiple flavors and package sizes distributed nationwide.

Several Tylenol products distributed by Gold Star Distribution Inc. were stored in conditions where rodents were present at their distribution center. This poses a potential contamination risk. The recall affects multiple Tylenol formulations including 500 mg, Cold & Flu, Cold & Flu Severe, PM, and Sinus Severe products nationwide.

Pepcid Complete 25-count packages distributed by Gold Star Distribution Inc. were stored in conditions with rodent activity and other sanitary issues at their distribution center. This affects all unexpired lots distributed nationwide by this company.

Pepto Bismol 32-count packs distributed by Gold Star Distribution Inc. were stored in conditions that included rodent exposure and activity. The distributor did not maintain proper sanitation standards required for over-the-counter medicines. All lots still within expiration date are affected.

Children's Nyquil Cold & Flu (Berry flavor, 8 oz bottles) distributed by Gold Star Distribution has been recalled due to insanitary conditions, including rodent activity, found in their distribution center. All unexpired lots distributed by this company are affected. No injuries have been reported.