State
20,371 recalls have nationwide distribution and so reach Missouri. 0 additional recalls listed Missouri 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 Missouri 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.
Stryker 2.3mm Tapered Router (craniotomy instrument) may break due to undersized core, leaving metal fragments in the surgical site. This risks damage to critical brain structures or need for additional surgery.
Jubilant Cadista Pharmaceuticals is recalling 28,560 bottles of Irbesartan 75 mg tablets nationwide due to failed dissolution specifications that may compromise drug efficacy.
Medline has recalled custom neurosurgical procedure kits nationwide due to leaking bottles of isopropyl alcohol. The leakage poses a risk of contamination and chemical exposure during surgical procedures.
The FDA is recalling 277 Fresenius AquaC UNO H dialysis machines due to misaligned internal ethernet cables that could expose the external port to electrical current, creating a shock risk for service technicians.
Teva Pharmaceuticals is recalling testosterone gel lot 1403180 after stability testing revealed out-of-specification assay results indicating superpotency. The affected 12,354 cartons were distributed nationwide.
The Sight OLO automated hematology analyzer displays mixed-up default reference ranges for children ages 2-11 in software versions 2.63, 2.63.1, and 2.63.1.1, which could cause test results to appear incorrectly normal or abnormal.
Medline is recalling medical convenience kits distributed nationwide that contain leaking bottles of isopropyl alcohol. Users should stop using the affected kits.
Medline Convenience surgical kits containing leaking bottles of isopropyl alcohol are being recalled nationwide. The leaking alcohol poses a risk of chemical exposure to healthcare workers and potential contamination of the surgical field.
Dr. Reddy's Laboratories is recalling Lansoprazole 15-mg delayed-release tablets nationwide due to failed dissolution specifications. The tablets may not dissolve properly, potentially affecting medication effectiveness.
Medline is recalling LAP CHOLE convenience kits due to leaking bottles of isopropyl alcohol. The affected kits were distributed nationwide.
Jubilant Cadista is recalling 9,600 bottles of Irbesartan Tablets (150mg) nationwide due to failed dissolution specifications. Affected lot IB220023A expires 08/2022.
Touch US Llc recalled 149 etouchus blood glucose meters (model ETM-G01) because they were marketed without FDA 510(k) clearance or approval. The device was distributed nationwide.
Medline convenience kits containing leaking bottles of isopropyl alcohol are being recalled. Approximately 477 units were distributed nationwide and should not be used.
Medtronic is recalling three Cobalt Implantable Cardioverter Defibrillators (CRT-D) due to a manufacturing error that may have resulted in a cathode component being out of specification. Affected patients should contact their physician.
Medline Industries is recalling medical device kits nationwide due to leaking isopropyl alcohol bottles. Approximately 28,745 units are affected. Consumers should stop using affected kits and contact the manufacturer.
Zeiss is recalling ZEISS Axio Observer 5 microscopes due to an incorrect Unique Device Identification (UDI) label installed on some units. The labeling discrepancy affects device tracking and identification.
Tiffin is recalling 2018-2022 Allegro and Allegro Breeze motorhomes where an improperly secured electrical buss bar can cause the DC Distribution Panel to overheat and potentially start fires. Dealers will replace the buss bar with a cable for free.
Holiday House is recalling certain 2019-2021 travel trailers with defective propane regulators that may fail and increase propane pressure, enlarging gas appliance flames and creating a fire risk. Dealers will replace the regulator free of charge.
Commercial trucks from multiple manufacturers may have incorrectly tightened brake caliper mounting bolts, reducing braking effectiveness. Daimler Trucks North America will notify owners for free inspection and repair.
Pending LLM rewrite. Source: NHTSA 21V015000.
Daikin Comfort Technologies is recalling about 298,300 evaporator coil drain pans that can overheat, melt, and deform, creating a fire hazard. The company has received 26 fire reports, with no injuries reported.
NUK First Choice 240 mL glass baby bottles sold on Amazon.com from January 2018 to May 2022 contain lead markings that exceed the federal lead content ban. Lead is toxic to young children if ingested.
Black Diamond Equipment is recalling about 76,300 avalanche transceivers that may fail to switch from SEND mode to SEARCH mode, preventing rescuers from locating buried skiers and risking severe injury or death.
Adventure Sports is recalling about 1,950 ceramic pulleys used in Cabrinha Switchblade and Drifter kiteboarding kites because the pulleys can cause bridle line breakage, reducing steering and control and risking kiteboarder injury.
Ocean Technology Systems is recalling about 500 underwater communication devices (PowerCom and MilCom models) with RBLi-4 lithium battery packs because water can leak into the battery pack and cause the circuit board to short and ignite after diving, posing a fire hazard.