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American Regent Inc. is recalling one lot of BetaVet, a betamethasone injectable suspension for intra-articular use in horses, sold in 5 mL single-dose vials. The vial crimps or seal may be loose or defective, which could affect the container's integrity. The recall covers lot 26038L2C1 (expires July 2027) and was distributed nationwide; no injuries have been reported.

Moderate·FDA·Oct 28, 2026

Wedgewood Pharmacy is recalling certain compounded veterinary medications shipped between February and October 2026 because lab testing data was unreliable, meaning some products may be weaker or stronger than intended. The affected medications include powders, pastes, oral liquids, injectables, and topical products for companion, equine, exotic, zoo, and aquatic animals. Wedgewood discovered the issue through its own quality checks and has received 98 complaints, including 7 serious ones.

Moderate·FDA·Oct 21, 2026·Wedgewood Pharmacy

Cronus Pharma is recalling one lot of AnaSed Equine Injection (xylazine 100 mg/mL), a sedative for horses, due to reports of product discoloration. The affected lot is C25110AV1 with an expiration date of November 2027. Discoloration may indicate a quality issue with the medication.

Moderate·FDA·Oct 20, 2026·Cronus Pharma

PHP Animal Health Pet Drops lubricant eye drops may not be sterile due to a manufacturing issue. The affected products are single 15 mL bottles and twin packs distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 8, 2026

Some Criticare nGenuity Patient Monitors with CO2 monitoring display a "Checkline Error" alarm during setup, which disables the CO2 monitoring function. This may delay medical procedures that rely on this monitoring capability.

Moderate·FDA·Sep 30, 2026·Criticare

C.R. Bard Inc. is recalling multiple SureStep Foley and Intermittent Catheter Tray Systems because the pericare wipes included in these kits may have contamination on their surface. The company received complaints about contaminated wipes in specific lot numbers distributed in the U.S., Canada, and several other countries.

Moderate·FDA·Sep 16, 20266 products

American Regent, Inc. Animal Health recalled four specific lots of Adequan Canine Injection (for dogs) and Adequan i.m. Injection (for horses) after discovering glass fibers in the products during internal testing. No adverse events have been reported to date.

Moderate·FDA·Jul 31, 2026

GO Raw LLC is expanding a recall of freeze-dried chicken pet food due to potentially low levels of thiamine (vitamin B1). Cats and dogs eating this food over time may develop deficiency symptoms ranging from decreased appetite and vomiting to neurological problems like neck bending, poor coordination, and seizures.

Moderate·FDA·Jun 8, 2026·GO Raw

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.

Moderate·FDA·May 27, 2026·Llorens

Tornier, Inc. recalled three shoulder implant parts that were incorrectly labeled as compatible with the Tornier HRS Max system. These parts actually work only with the older Tornier HRS system and will not fit properly in HRS Max procedures. A total of 233 units with specific lot numbers were distributed nationwide.

Moderate·FDA·Apr 15, 2026·Tornier

Valley Springs/Artesian Gold recalled three 1-gallon water products sold as Valley Springs 100% Natural Bottled Water (including a fluoride-added version) and Valley Springs Steamed Distilled Water. The water was bottled under insanitary conditions. The products were distributed in Illinois and Wisconsin, and no injuries have been reported.

Moderate·FDA·Mar 4, 2026·Valley Springs Artesian Gold3 products

Medline Industries recalled multiple surgical drape products due to calibration problems with sterilization equipment. While the drapes went through sterilization and packaging, equipment calibration issues may have compromised their sterility. No injuries have been reported.

Moderate·FDA·Feb 25, 202642 products

Bard Peripheral Vascular is recalling multiple central venous catheter trays and kits because the outer packaging may be damaged, which could compromise the sterile barrier that protects the medical device. The recall affects several Broviac and Hickman catheter products with specific lot numbers manufactured between April 2028 and August 2030.

Moderate·FDA·Feb 25, 2026

Fujirebio is recalling seven Lumipulse plasma test products used to measure amyloid and pTau217 for Alzheimer's disease. The tests can produce falsely elevated results, which may wrongly classify a patient as having Alzheimer's-related amyloid pathology or lead to unneeded additional testing. No injuries have been reported.

Moderate·FDA·Feb 11, 2026·Fujirebio7 products

Vortex Surgical laser probes used in eye surgery may have small voids or gaps in their sterile packaging seals. If the seal is compromised, bacteria could contaminate the sterile device and cause infection during surgery. No injuries have been reported so far.

Moderate·FDA·Feb 11, 2026·Vortex Surgical13 products

Certain GE Healthcare Omni Legend PET scanners may occasionally produce streaking artifacts in scan images. This visual distortion appears as lines in the images displayed on the scanner console and could affect image quality used for clinical diagnosis.

Moderate·FDA·Jan 28, 2026

Copan is recalling two versions of its 1 ml DTT liquid-phase transfer tubes used to liquefy respiratory specimens, covering 245,700 units in total. The company cannot guarantee the treatment reagent will work properly, so specimen liquefaction may not be reliable. The tubes were distributed to 14 states, and no injuries have been reported.

Moderate·FDA·Dec 24, 2025·Copan2 products