State
73,566 recalls have nationwide distribution and so reach Wyoming. 3,226 additional recalls listed Wyoming specifically in their distribution scope.
Of the 3,226 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 681 (21%) are Severe.
Which agencies issued them
These figures cover only the 3,226 recalls whose distribution notice names Wyoming specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medtronic Xomed is recalling over 301,000 NIM TRIVANTAGE EMG Endotracheal Tubes due to a manufacturing nonconformity. These devices were distributed worldwide.
Philips Allura CV20 X-ray systems with certain Laird chillers may leak cooling liquid onto electrical components, potentially causing fire or smoke. Affected systems should not be operated until the issue is addressed.
RayStation/RayPlan versions 6.0.0.24 through 9.2.0.483 incorrectly display selected images as both primary and secondary when animation playback is running, affecting treatment planning visualization.
Philips Allura Xper interventional X-ray systems may experience cooling liquid leaks that could drip on electrical components, creating risk of fire, smoke, or burning odors. No injuries have been reported.
NeuMoDx COVID-19 test strips (Lot 116305 S/L-02) are recalled due to product contamination that increases risk of false positive results. The recall affects 102 boxes distributed in FL, MD, MI, and NY.
Nextremity Solutions recalls the Nextra CH Hammertoe Mini Instrument Kit for a defect that may deform the implant's locking mechanism during insertion, potentially requiring revision surgery.
A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.
B. toys Walk 'n' Learn wooden toddler walkers are being recalled because wheels and attachment hardware can detach in small pieces, creating a choking hazard for young children. Battat has received six reports of detachment, including one incident where a child placed a detached metal nut in her mouth.
Volkswagen is recalling certain 2021 ID.4 vehicles due to improper soldering of the high-voltage battery connection. The defect may cause an unreliable connection that could lead to vehicle stalling and increase crash risk.
El Chavito Saladitos Enchilados Salted Plums (1.7 oz.) are being recalled nationwide due to potential lead contamination. Consumers should not consume this product.
The Nextra Cannulated Hammertoe Standard Instrument Kit's driver may deform the implant locking mechanism during insertion, potentially requiring revision surgery.
RB Health (Reckitt) is recalling approximately 3.74 million bottles of Airborne Gummies (63 and 75 count) because pressure buildup can cause the cap and seal to pop off with force upon first opening, posing an injury hazard.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry VersaTips due to shape deformity that may reduce sample volume by 16%. Undetected errors could result in inaccurate test results for bloodborne infectious disease assays.
El Chavito Saladitos Dried Salted Plums are being recalled due to potential lead contamination. The recall affects 37,552 packages distributed nationwide.
Prestone has recalled Shop Pro RV & Marine Antifreeze sold at AutoZone after discovering some bottles were improperly filled with methanol-containing product and lack required hazard warnings. Methanol can cause poisoning through inhalation or ingestion and may be fatal or cause blindness.
Stryker is recalling the 1688 Camera Control Unit due to a software defect that causes the surgical monitor image to flip upside-down. This could lead to surgeon error or the need for additional surgical intervention.
Envisiontec is recalling 172 PCA 4000 curing units that may not properly cure dental resins to specification (SKU ACC-06-1000).
Specialized is recalling about 19,000 Sirrus bicycles with defective alloy cranks that can disengage and cause falls. The manufacturer has received 30 reports of the defect, but no injuries have been reported.
RH is recalling about 3,300 illuminated mirrors sold from September 2015 through February 2022 due to loose components in bulb sockets that can cause overcurrent, overheating, fire, and electrical shock. Consumers should stop using them immediately and contact RH for a refund or replacement.
Coca-Cola Cherry Zero Sugar 12-packs distributed in AZ, UT, and WY are being recalled because individual cans lack required phenylketonuric (PKU) warning labels, which are necessary for people with phenylketonuria.
Harley-Davidson is recalling certain 2021-2022 XL Sportster motorcycles because brake fluid warning labels may detach from reservoir caps. Missing labels could lead to improper brake maintenance and increased crash risk.
The Harvard Drug Group is recalling 174 cartons of Paliperidone Extended-Release Tablets, 9 mg, nationwide due to failed dissolution specifications. The affected lots are N00522 (Exp. 09/2022) and N00618 (Exp. 11/2022).
Carl Zeiss Meditec is recalling CIRRUS HD-OCT Models 5000 and 6000 AngioPlex devices. The optic nerve head angiography feature was distributed without FDA pre-market clearance and must be disabled.
3-D Matrix, Inc. is recalling PuraSinus Absorbable Nasal Hemostat units because the shipping boxes used for transport were not validated.
Kia is recalling 2014-2016 Cadenza vehicles because the front windshield may not be properly bonded, posing a risk of detachment.