State
20,371 recalls have nationwide distribution and so reach Colorado. 0 additional recalls listed Colorado specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Colorado consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Hobbs Medical is recalling Hobbs Posi-Stop Injection Needles due to incorrect expiration dates on device labels that extend the shelf life. Affected devices have lot numbers ending in 'R' distributed from 2018–2020.
Hobbs Medical is recalling the Freeman Pancreatic Flexi-Stent Kit because the device label displays an incorrect expiration date that extends the shelf life. U.S. distribution of affected devices occurred between March 25, 2018 and September 28, 2020.
Hobbs Medical, Inc. is recalling Hobbs Helical Retrieval Baskets with lot numbers ending in R due to incorrect expiration dates on device labels. Affected units were distributed worldwide from March 2018 to September 2020.
Baxter Healthcare recalls Prismaflex HF Set devices due to a mistranslation in Estonian language instructions. The mistranslation contains contradictory information about patient body weight restrictions.
Hobbs Medical is recalling Helical Retrieval Baskets due to incorrect expiration dates on device labels. The mislabeling extends the shelf life, potentially allowing use of expired devices.
Hobbs Medical is recalling Cytology Brush Catalog Number 4206 due to incorrect expiration dates on product labels that extend the intended shelf life. Approximately 300 units were distributed nationwide and internationally between March 2018 and September 2020.
Hobbs Medical is recalling polypectomy snares with incorrect expiration dates on labels. Affected devices have lot numbers ending in R and were distributed from March 2018 to September 2020.
LUMINOSTICS recalled Clip COVID test kits because the manufacturer extended shelf life and expiration dates without FDA approval. The extended expiration dates lack FDA validation.
BRP is recalling certain 2022 Ski-Doo snowmobiles with 850 E-TEC engines due to a loose fuel injector hose retainer screw that can cause fuel leaks and fires. The company has received five fuel-leak reports, resulting in two fires.
U-Line is recalling about 90 Outdoor Series 24-inch built-in convertible freezers that can overheat and pose a fire hazard. U-Line has received three reports of freezer fires with no injuries reported.
About 22,000 Ancheer e-bikes with lithium-ion batteries are being recalled because the batteries can ignite, explode, or spark, causing fire and burn injuries. Consumers should stop using the recalled bikes immediately and contact Ancheer for a free replacement battery and mount.
Ekouaer children's bathrobes fail to meet federal flammability standards for sleepwear, posing a burn risk to children. About 9,200 units sold on Amazon between March 2020 and July 2021 are affected.
Addo Play has recalled about 9,300 Early Learning Centre Little Senses Lights & Sounds Shape Sorter Toys sold on Amazon from October 2020 through August 2022. The red cube can detach during use and release a small white ball, posing a choking hazard to infants.
U.P. Fashion is recalling approximately 1,800 children's rings sold nationwide at dollar stores and discount stores from April 2021 through July 2022 because the metal base contains lead levels exceeding the federal lead content ban.
Cressi-Sub USA is recalling about 1,350 scuba buoyancy compensator devices (BCDs) with defective inflator hoses that may fail to inflate properly, posing a drowning hazard to divers.
Jammers Apparel Group is recalling about 450 children's nightgowns sold at JCPenney from March to May 2022 because they fail to meet federal flammability standards and pose a burn risk to children.
Newair is recalling about 11,750 Magic Chef Air Fryers because they can overheat, posing fire and burn hazards. Consumers should stop using them immediately and contact Newair for a refund.
Philips Respironics is recalling Wisp and Wisp Youth nasal masks because they lack warnings about magnetic components that could interfere with implanted medical devices or cause eye injuries from metallic splinters.
Philips Respironics is recalling 930,813 DreamWisp Nasal Masks worldwide due to missing warnings about magnetic components that could interfere with implantable medical devices or cause metallic splinters.
Philips Respironics Amara View Full-Face Mask lacks critical safety warnings about magnetic components for patients with implantable medical devices. The Class I recall affects 5.6 million units worldwide.
Pending LLM rewrite. Source: FDA_DRUG D-0007-2023.
Pending LLM rewrite. Source: FDA_DEVICE Z-1781-2022.
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Pending LLM rewrite. Source: FDA_DEVICE Z-1784-2022.
Pending LLM rewrite. Source: FDA_DRUG D-1551-2022.