South Dakota recalls

Novocol Pharmaceutical issued a recall of 2% Xylocaine Dental with Epinephrine 1:100,000 injection cartridges due to defective containers—some cartridges are cracked or broken. This affects lot D05337B (expires 06-30-2027). The problem was discovered during quality control; no injuries have been reported.

Olympia Provisions is recalling about 1,930 pounds of ready-to-eat holiday kielbasa sausage because metal fragments may be in the product. The sausages were produced on October 14, 2025, and sold in 16-ounce packages with a "best if used by" date of 02/19/26. No injuries have been reported so far.

Meaicezli Play Purse Sets contain toy cell phones and writing tablets with button or coin cell batteries that children can easily remove and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.

Blue Wave above-ground pools 48 inches and taller have a compression strap around the outside of the pool legs that can act as a foothold, allowing children to climb into the pool unsupervised. This creates a serious drowning risk. The strap can provide access to the pool even if you remove the ladder.

ANNQUAN power strips (models EX-D112-05 and EX-D106-25) lack proper safety protection and can overheat and catch fire if overloaded. Seven units have blown fuses. The fire risk can cause serious injury or death from burns and smoke.

JOKOSIS bed rails (model HC0262) can trap users between the rail and mattress, creating a serious risk of entrapment and asphyxiation. The rails also lack required warning labels. About 12,000 units were sold on Amazon between August and November 2025.

KKL Fabric 9-Drawer Dressers can tip over and trap children if not anchored securely to the wall. The dressers do not meet federal safety standards for clothing storage units. About 4,740 units were sold on Amazon between September 2023 and November 2025.

Feel The Beard Beard Growth Oil contains minoxidil, a medication that must be in child-resistant packaging by law. The bottles do not have child-resistant caps, which means young children could open them and swallow the contents, causing serious injury or death. The product was sold online from April through September 2025.

Mamisan Pain Relieving Topical Ointment contains lidocaine but does not have child-resistant packaging as required by law. Young children could open the jar and swallow the contents, causing serious injury or death. The recalled product is in a 3.52 ounce orange plastic jar with a white lid and UPC code 860006498115.

These 18-drawer dressers can tip over and trap children if not anchored to the wall. The dressers have a metal frame, wooden top, and fabric drawers, and were sold in black, brown, and gray. They fail to meet mandatory safety standards for furniture stability.

Currey & Company Electra Chandeliers have a defective ceiling connection that may not be threaded properly. This can cause the heavy fixture to fall unexpectedly. Two fixtures have already fallen; one caused property damage.

TopHomer 8-inch pool drain covers do not meet federal safety standards and can trap swimmers or bathers, creating a drowning risk. The covers were sold on Amazon from August 2024 through October 2025. No injuries have been reported, but the hazard is serious.

Furnulem 8-Drawer Dressers can tip over and trap children if not anchored to the wall. These dressers were sold on Amazon from September 2023 through November 2025. The dressers fail to meet federal safety standards for furniture stability.

Pedego electric tricycles can develop hairline fractures in the frame near a weld, causing the tubes to separate. This poses a risk of falling off the trike and being cut. The company has received 16 reports of frame breakage, including one injury.

The buckles that secure the restraint straps on this rear-mounted bike carrier can release during use, which could cause a child to fall. Pacific Cycle has received one report of buckle failure, though no injuries have been reported yet.

The arm on Amp Fit's MP2 Smart Fitness Machine can swing unexpectedly because the locking mechanism does not hold securely. The company has received 10 reports of injuries, including lacerations to the head and bruising to the shoulder and other areas.

Stryker recalled certain Arise 1000EX mattresses because some were sold near MV3 beds, raising concern they might be used together. The mattress and bed have not been tested together and are not designed to work as a pair. Using them together is not recommended by Stryker.

Stryker recalled certain MV3 bariatric beds because some were sold near Arise 1000EX mattresses, suggesting they might be used together. The bed and mattress have not been tested for compatibility and should not be used together.

Datascope Corp. is updating the maintenance schedule for Cardiosave Rescue intra-aortic balloon pump systems to match changes made to the Service Manual in June 2023. This affects 47 units distributed worldwide. No injuries have been reported.

Datascope Corp. has updated the preventative maintenance schedule for Cardiosave Hybrid intra-aortic balloon pump systems to match changes made to the Service Manual in June 2023. Users should review the updated Instructions for Use (IFU) addendum to ensure proper maintenance timing.

A screw in certain Nipro Surdial DX hemodialysis systems may loosen or fall out during use. This is a medical device used in dialysis treatment. The affected units have specific serial numbers issued between 2020 and 2024.

Medline Industries is recalling DEXLOCK Achilles Repair Implant Kits (model MAKT4520, lot 19019) because the drill bit can fuse to the drill guide during surgery. This can delay the procedure while a replacement drill bit and guide are retrieved. No patient injuries have been reported.

A wire inside the AMSCO 7053HP Washer/Disinfector may shift out of position and cause electrical arcing within the unit. The arcing occurs inside the machine and does not pose a shock risk to users. This affects 22 units with specific serial numbers distributed in the US and Australia.

A wire in the electrical box of the AMSCO 7052HP Washer/Disinfector may shift out of position, causing electrical arcing inside the unit. The arcing occurs internally and does not pose a shock risk to users, but could affect equipment function or safety.

C.R. Bard Inc. has recalled certain BD InLay Optima Ureteral Stent Kits (8 Fr. x 26 cm, REF 78826, Lot# NGJU4328) because the actual stent size may not match what the label says. This labeling error could lead to incorrect stent selection during medical procedures.

C.R. Bard Inc. is recalling a specific lot of BD InLay Optima Ureteral Stent Kits (6 Fr. x 30 cm, Ref 788630, Lot NGJU4327) because the actual stent size may not match what is printed on the product label. This discrepancy could affect proper stent selection and placement.

BD InLay Optima Ureteral Stent Kits (4.7 Fr. x 26 cm, Lot NGJU4181) have a labeling error—the printed size on the package may not match the actual stent inside. This affects 4,350 units distributed across multiple U.S. states and internationally. No injuries have been reported.

C.R. Bard Inc. is recalling certain InLay Optima ureteral stent kits (6 Fr. x 14 cm, REF 787614, Lot# NGJU4163) because the actual size of the stent may not match what is printed on the package label. This discrepancy could affect proper medical placement and treatment.

Medline has found that Quick Strip Fabric Sterile Adhesive Bandages (1" x 3") may have open or damaged seals on their packaging. When the seal is compromised, the sterility of the bandages inside cannot be guaranteed. This affects all lots of the product.