Colorado recalls

Sold nationwide. Beestech spiral tower toys sold on Amazon contain small plastic balls and are marketed for children under 3 years old, violating federal toy safety rules. The small balls pose a serious choking hazard. About 200 units were sold between November and December 2025.

Serious·CPSC·Apr 2, 2026·Beestech

Sold nationwide. Medline Industries has recalled specific lots of Puracol and Puracol Plus collagen wound dressings due to elevated endotoxin levels. These contaminants can cause inflammation, tissue irritation, delayed healing, fever, low blood pressure, and in severe cases, septic shock.

Serious·FDA·Apr 1, 2026·Medline

Sold nationwide. The labeling on BD Alaris System with Guardrails Suite MX does not specify which version of Transport Layer Security (TLS) must be enabled on hospital networks for secure Wi-Fi communication with Point-of-Care Units. This could create confusion during setup and potentially leave devices with inadequate security settings.

Moderate·FDA·Apr 1, 2026·CareFusion

Sold nationwide. Olympus is recalling seven models of bipolar and PK/PKS cutting forceps, 3,788 units in total, used in medical procedures. The supplier did not adequately validate a welding process for components, and defective welds could cause the forceps' jaw to break during clinical use. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·Olympus7 products

Sold nationwide. Tandem Diabetes Care insulin pumps distributed in the Czech Republic and Slovakia have translation errors in their Czech language user guide. The most serious error tells users to verify the infusion set is connected to the body when it should say the opposite—that it should NOT be connected. Following these incorrect instructions could cause unintended insulin delivery and dangerously low blood sugar.

Moderate·FDA·Apr 1, 2026·Tandem Diabetes Care

Sold nationwide. Medtronic has recalled certain MiniMed 780G insulin pumps due to software defects that can cause the pump to deliver too much insulin, too little insulin, or stop delivering insulin entirely. These defects appeared after software updates (versions 6.60, 6.61, and 6.62) and may result in dangerously high or low blood sugar levels. The recall affects over 26,000 pumps with specific serial numbers.

Serious·FDA·Apr 1, 2026·Medtronic

Sold nationwide. AMO has recalled certain TECNIS Eyhance intraocular lenses (IOLs) used in cataract surgery because a small number may have a defect where the lens haptic (support arm) sticks to the optic, preventing proper unfolding during implantation. This affects 361 lenses distributed across 12 U.S. states. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·AMO

Sold nationwide. Straumann is recalling two custom abutment products, 20 units in total, for dental implant use. A raw material bar of TAN material was mislabeled as titanium Grade 4, so some RC Titanium abutments were made from the wrong material. The affected units were distributed in several U.S. states and in Canada. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·Straumann2 products

Sold nationwide. Koven Technology's BiDop 3 Pocket Doppler ultrasound device was distributed with labeling that claims it can be used for fetal applications, but the FDA never approved it for that use. The device is only cleared to detect blood flow in blood vessels, not for fetal monitoring. Using it for unapproved purposes could lead to incorrect results or missed diagnoses.

Moderate·FDA·Apr 1, 2026·Koven Technology

Sold nationwide. Orthalign drill plates (Trimax-Pegged, Sizes 1–5, REF 402566) in one lot may have been made outside specifications. This could cause bone cuts larger than intended during knee surgery. Seven units were distributed in Utah.

Moderate·FDA·Apr 1, 2026·Orthalign2 products

Sold nationwide. Philips is recalling 11 ultrasound transducer models to clarify and update labeling that defines how long these devices are expected to remain in use. The recall was filed for clarification, and no injuries have been reported.

FDA·Apr 1, 2026·Philips11 products

Sold nationwide. Philips is recalling four Trilogy ventilator models running software version 1.05.15.00: Trilogy Evo, Trilogy Evo O2, Trilogy EV300, and Trilogy Evo Universal. When non-pneumatic nebulizers are used with these ventilators, the breath volume the patient receives may differ from the amount the device is set to deliver. No injuries have been reported. The recall covers about 113,717 units per model and was distributed nationwide and in many other countries.

Serious·FDA·Apr 1, 2026·Philips4 products

Sold nationwide. Olympus is recalling four endoscope products because the MAJ-1443 and MAJ-1444 valves are no longer compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. The recall covers about 139,000 units across the US, and no injuries have been reported.

Moderate·FDA·Apr 1, 2026·Olympus4 products

Sold nationwide. Beckman Coulter has recalled MicroScan Neg MIC 56 antimicrobial susceptibility testing panels (Catalog C42464, Lot 2026-01-03) due to potential contamination in the test wells. These panels are used by laboratories to identify bacteria and test antibiotic resistance. Contaminated panels could produce inaccurate test results.

Moderate·FDA·Apr 1, 2026·Beckman Coulter

Sold nationwide. I.T.S. is recalling 17 orthopedic implant product lines, including bone plates and screw systems. Updated MRI safety testing found that these implants can heat up more during certain MRI conditions than the product instructions previously stated. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·I.T.S17 products

Sold nationwide. GE Medical Systems' Imactis CT-Navigation System (Models E85101LA and E85101LP) has a potential issue where the needle's simulated path shown to the doctor may not match where the needle actually goes during CT-guided procedures. This discrepancy could affect the accuracy of needle placement during medical procedures. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·GE

Sold nationwide. The Handy Solutions Neck & Shoulders Heating Pad (model 25607) can overheat and cause burns if folded while in use or placed under your body. When folded, the device's safety temperature sensor cannot detect the excessive heat, so it does not shut off. The pad may emit a burning smell before melting or catching fire.

Serious·FDA·Apr 1, 2026·Navajo Manufacturing

Sold nationwide. Merit Medical is recalling five products, including CentrosFLO and DuraMax dialysis catheters and 16F dual valved splittable sheath introducers. The sheath introducer may not split as intended, which can cause bleeding, pieces left in the body, procedure delays, or blood clots. No injuries have been reported.

Serious·FDA·Apr 1, 2026·Merit Medical5 products

Sold nationwide. Erbe is recalling three models of flexible cryoprobes used in surgery because the probes may rupture or burst during activation. The recall covers about 40,900 units sold nationwide, including Puerto Rico. No injuries have been reported.

Serious·FDA·Apr 1, 2026·Erbe3 products

Sold nationwide. Nuts.com Espresso Malted Milk Balls contain wheat and soy allergens that are not listed on the package label. The ingredient soy lecithin contains soy, and wheat is also present in the product. People with wheat or soy allergies could have a serious reaction if they eat this product.

Serious·FDA·Apr 1, 2026·Nuts.com

Savannah Bee Company is recalling certain bottles of Honey BBQ Sauce labeled as "Mustard" because they actually contain the "Sweet" variety inside, which has undeclared soy and wheat allergens. The mislabeled bottles pose a serious risk to people with soy or wheat allergies. The affected product has UPC 8 50033 93758 9 and a best-before date of 05/16/27.

Moderate·FDA·Apr 1, 2026·Savannah Bee Company

Sold nationwide. Sunflour Bakery hamburger buns contain sesame seeds that are not listed on the package label. One 18-ounce bag (UPC 832971001522) with an expiration date of 02/24/2026 was distributed to a retailer in Orange County. People with sesame allergies could have a serious reaction if they eat these buns.

Moderate·FDA·Apr 1, 2026·Sunflour Bakery

Sold nationwide. Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

FDA·Apr 1, 2026·Herbal Creations USA

Ajinomoto is recalling 11 fried rice and gyoza dumpling products because they may contain pieces of glass, 1 to 3 cm long and 2 to 4 mm wide. The products are sold under the Trader Joe's, Kroger, Ajinomoto, Ajinomoto Ling Ling, Tai Pei and Golden Tiger names and were distributed in 43 states. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·Trader Joe's11 products

Sold nationwide. Western Mixers is recalling two sizes of Chilli Spanish Peanuts because glass was found inside sealed containers. The products are sold under the First Street brand (11 oz containers) and the Treasured Harvest brand (25 lb bags). No injuries have been reported. The recall was sent to two businesses with a total of 53 retail locations nationwide.

Moderate·FDA·Apr 1, 2026·First Street2 products

Sold nationwide. American Health Packaging is recalling specific batches of Meclizine Hydrochloride 12.5 mg tablets because they failed to meet required tablet specifications. The affected product is Lot #1024852 with an expiration date of 9/30/2026. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·Amerisource

Sold nationwide. Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension due to sterility concerns identified at the manufacturing facility. The FDA found quality system deficiencies that could affect the safety of the medication.

Moderate·FDA·Apr 1, 2026·Teva3 products

Sold nationwide. Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.

Moderate·FDA·Apr 1, 2026·MacLeods Pharma

Sold nationwide. Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.

Moderate·FDA·Apr 1, 2026·Chiesi

Sold nationwide. Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.

Moderate·FDA·Apr 1, 2026·Radnostix