State

Wyoming product recalls

20,371 recalls have nationwide distribution and so reach Wyoming. 0 additional recalls listed Wyoming specifically in their distribution scope.

About recalls in Wyoming

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 Wyoming 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.

12451–12475 of 20371

ModerateFDA (Drugs)·D-0927-2023·2023-07-26
FDA Recalls Phenylephrine HCl IV Solution Over Manufacturing Contamination
Advanced Compounding Solutions is recalling 82 bags of phenylephrine HCl intravenous solution due to potential contamination from manufacturing facility violations. No illnesses have been reported.
Product
PHENYLephrine HCl 10mg added to 0.9% Sodium Chloride 250mL, 250 mL IV Bag @60 Total volume), RX only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042, NDC: 71546-450-25;
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2146-2023·2023-07-26
Aesculap Surgical Needle Recalled for Incorrect Product Code Marking
Aesculap Implant Systems is recalling Aesculap Surgical Needles (MD610) because they are etched with an incorrect product code. The needles are marked MD611 when they should be marked MD610.
Product
Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0939-2023·2023-07-26
Famotidine tablets recalled for carton labeling error on strength
Glenmark Therapeutics is recalling famotidine 20 mg tablets after some cartons were labeled with a side label indicating 10 mg instead. The medication inside is correct; only the external carton label is mislabeled.
Product
FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0924-2023·2023-07-26
Loteprednol Etabonate Eye Drops Recalled for Out-of-Specification Potency
Sun Pharmaceutical recalls Loteprednol Etabonate eye drops due to out-of-specification unit dose content in certain lots. Affected bottles may contain incorrect potency levels.
Product
LOTEPREDNOL ETABONATE — LOTEPREDNOL ETABONATE (LOTEPREDNOL ETABONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0925-2023·2023-07-26
Prescription drug recall: Fingolimod capsules fail dissolution specifications
Ascend Laboratories is recalling 2,652 bottles of Fingolimod capsules nationwide because they failed to meet dissolution specifications, potentially affecting medication effectiveness.
Product
FINGOLIMOD — FINGOLIMOD (FINGOLIMOD HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighCPSC·23774·2023-07-20
CUPKIN Stainless Steel Children's Cups Recalled for Excessive Lead Content
SOOJIMUS is recalling about 346,000 CUPKIN Double-Walled Stainless Steel Children's Cups because they contain lead levels that exceed the federal ban. Lead ingestion poses a health risk to young children.
Product
CUPKIN Double-Walled Stainless Steel Children's Cups
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23247·2023-07-20
Wild Country Superlight Rocks climbing chocks recalled for fall hazard
Salewa USA recalls Wild Country Superlight Rocks cable wire climbing chocks due to corrosion from seaside exposure that weakens and breaks the chocks, creating a fall hazard for climbers. No injuries have been reported in the U.S.
Product
Superlight Rocks
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23775·2023-07-20
Pottery Barn Kids Penny Convertible Cribs Recalled for Laceration Hazard
Williams-Sonoma Inc., operating as Pottery Barn Kids, is recalling about 310 Penny Convertible Cribs because the end panel can become loose and expose sharp edges, creating a laceration hazard to children. No injuries have been reported.
Product
Pottery Barn Kids Penny Convertible Cribs
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1242-2023·2023-07-19
Multiple Pretzel Brands Recalled for Undeclared Milk Allergen
Honey mustard pretzel products from multiple brands are being recalled due to potential undeclared milk. The recall affects 334,357 bags distributed nationwide.
Product
1. Hy-Vee Honey Mustard Braided Pretzels, 10oz poly bags, UPC: 75450-24309, 12 pack; 2. Dakota Style Honey Mustard Pretzel Kravings, 10oz poly bags, UPC 84872-60031, 12 pack and 6 pack; 3. Four Brothers Honey Mustard Pretzels, 10oz poly bags, UPC: 33147-89145, 12 pack; 4. Schn
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0938-2023·2023-07-19
Prescription albuterol inhalers recalled nationwide due to defective valve seals
Cipla USA is recalling 278,538 albuterol sulfate inhalers nationwide with specific lot numbers due to defective valve gaskets that cause empty inhalers or medication leakage. Check your lot number and contact your healthcare provider if affected.
Product
ALBUTEROL SULFATE — ALBUTEROL SULFATE (ALBUTEROL SULFATE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0921-2023·2023-07-19
Artificial Tears Eye Drops Recalled for Bacterial Contamination
Delsam Pharma's Artificial Tears eye drops are being recalled nationwide due to bacterial contamination found in unopened bottles. Consumers should stop using affected products immediately.
Product
Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2103-2023·2023-07-19
Baxter SIGMA Spectrum Infusion Pump false upstream occlusion alarm correction
Baxter is correcting false upstream occlusion alarms in SIGMA Spectrum and Spectrum IQ infusion pumps following software upgrades affecting approximately 3,306 units distributed nationwide in the US.
Product
SIGMA Spectrum Infusion Pump, Product Code 35700BAX2
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2104-2023·2023-07-19
Spectrum IQ Infusion System False Occlusion Alarm Correction Issued
The FDA has issued a Class I correction for Baxter's Spectrum IQ Infusion System due to increased false upstream occlusion alarms following software updates. Approximately 19,861 units are affected nationwide.
Product
The Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2018-2023·2023-07-19
Oxylog 3000 Plus ventilator may stop working during operation
The Draeger Oxylog 3000 Plus emergency and transport ventilator may stop working when transitioning from battery to AC operation. Approximately 300 units distributed nationwide and internationally are affected.
Product
Oxylog 3000 Plus emergency and transport ventilator
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1241-2023·2023-07-19
Pretzel products recalled for undeclared milk allergen nationwide
Dakota Style, Inc. is recalling salt and vinegar pretzel products nationwide because they may contain undeclared milk. Consumers with milk allergies should not consume these products.
Product
1. Hy-Vee Salt & Vinegar Braided Pretzels, 10 oz poly bags, UPC: UPC: 75450-27706, 12 pack; 2. Dakota Style Salt & Vinegar Pretzel Kravings, 4.5 oz poly bags, UPC: 84872-60030, 6 pack; 3. Dakota Style Salt & Vinegar Pretzel Kravings, 10 oz poly bags, UPC 84872-60018, 12 pack, 4
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1243-2023·2023-07-19
Multiple Brands of Dill Pickle Pretzels Recalled for Undeclared Milk
Dakota Style, Inc. is recalling multiple brands of dill pickle pretzels nationwide because they may contain undeclared milk, a major allergen. Consumers with milk allergies should not consume these products.
Product
1. Hy-Vee Dill Pickle Braided Pretzels, 10oz poly bags, UPC: UPC: 75450-24308, 12 pack; 2. Schnucks Dill Pickle Pretzel Schticks, 10oz poly bags, UPC: 41318-25268, 12 pack; 3. Best Choice Dill Pickle Pretzel Twists, 10oz poly bags, UPC: 700038-66480, 12 pack; 4. Gelson's Dill P
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2110-2023·2023-07-19
Abbott Cardiac Catheter Sheath Recalled Due to Air Embolism Risk
Abbott is recalling the Amplatzer Steerable Delivery Sheath (ASDS), a cardiac catheter, due to a 0.77% reported incidence rate of air embolism during procedures. The recalled 675 units are distributed worldwide.
Product
Abbott Amplatzer Steerable Delivery Sheath (ASDS), REF ASDS-14F-075, is a percutaneous catheter (cardiac).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0919-2023·2023-07-19
EzriCare Artificial Tears Eye Drops Recalled for Bacterial Contamination
EzriCare Artificial Tears eye drops are being recalled nationwide due to bacterial contamination found in unopened bottles. The FDA identified non-sterile products that could pose a risk to eye health.
Product
Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1244-2023·2023-07-19
Gelson's Sea Salt Pretzels Recalled for Undeclared Milk Allergen
Gelson's Sea Salt Pretzels are being recalled nationally because they may contain undeclared milk. This poses a hazard to consumers with milk allergies.
Product
Gelson's Sea Salt Pretzels, 4.5oz poly bags, UPC: 23631-11185, 12 pack
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2108-2023·2023-07-19
Osteomed AutoDrive Screws Recalled for Undersized Screw Head
Osteomed recalls orthopedic AutoDrive screws used in osteotomy procedures due to undersized screw heads that could pass through the mounting plate hole, potentially affecting surgical fixation.
Product
REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only, Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2107-2023·2023-07-19
Orthopedic Screw Recall Due to Undersized Head in Surgical Device
Osteomed is recalling orthopedic screws with undersized heads that may pass through bone plates. Affected lot numbers were distributed nationwide in the US and Singapore.
Product
REF: 218-1604, 1.6mm x 4mm Profile Zero Auto-Drive Screw, Rx Only, Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0902-2023·2023-07-19
Careone Allergy Relief tablets recalled for failed impurity and degradation specifications
Careone Allergy Relief fexofenadine hydrochloride 180mg tablets are recalled nationwide for failing impurity and degradation specifications. Lot 2JE2185 with expiration date 01/24 is affected.
Product
CAREONE ALLERGY RELIEF — CAREONE ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2134-2023·2023-07-19
Medline Non-Sterile PVP Solution Mislabeled as Sterile
Medline Industries is recalling 128 units of non-sterile PVP solution incorrectly labeled as sterile. Using a non-sterile product in sterile contexts could create infection risk.
Product
MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: OISC HAND BEAR, Model Number DYNJ902348L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0903-2023·2023-07-19
Allergy Relief Fexofenadine Hydrochloride Tablets Recalled for Failed Quality Specifications
CVS Pharmacy is recalling 16,200 cartons of Allergy Relief fexofenadine hydrochloride tablets nationwide due to failed impurities and degradation specifications. Stop using affected lot 2DV1925 and consult a pharmacist.
Product
Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 69842-0914-39
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2123-2023·2023-07-19
Medtronic Catalyft LS Spinal Implant Recalled for Out-of-Specification Geometry
Medtronic recalls Catalyft LS spinal implants due to potential out-of-specification dimensions. The affected devices may not properly fit or function as intended during spine fusion surgery.
Product
Medtronic Catalyft LS Expandable Interbody System Implant Kit, Anterior Standalone Cage, REF SPS03188, spinal implant kit
Category
Medical Device
Distribution
Distributed nationwide