Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,364 recalls have been distributed to Wyoming in the last 12 months.
Showing 30921–30940 of 48,219 recalls
Recalled Item: Mitomycin 0.02% (0.2 mg/mL) in Sterile Water for Injection (Injection)...
The Issue: Lack of Assurance of Sterility; all compounded products within expiry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kelloggs ¿ Eggo ¿ Nutri-Grain¿ Whole Wheat Waffles 12.3 oz Recalled by...
The Issue: Potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or...
The Issue: Issue with the process for detection of leaking Pressure Tourniquet Cuffs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee System Box Cut Guide The EMPOWER PS Recalled by Encore...
The Issue: It has been discovered that during Empowr PS Total Knee replacement, while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PeroxiClear Peroxide Solution Recalled by Bausch & Lomb Inc Irb Due to...
The Issue: Product was found to contain excess residual levels of hydrogen peroxide.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Club Size McCormick Original Taco Seasoning Mix 24 oz. Recalled by Mccormick...
The Issue: Product was recalled due to undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: National Foods Packaging Chicken Base in 25 lb white poly-lined paper bags...
The Issue: Product contains a spice which was tested and found to contain elevated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: National Foods Packaging Low Sodium Chicken Base in 50 lb Recalled by...
The Issue: Product contains a spice which was tested and found to contain elevated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags Recalled by...
The Issue: Product contains a spice which was tested and found to contain elevated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marcaine 0.25% (bupivacaine HCl) injection Recalled by Hospira Inc., A...
The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Marcaine 0.5% (bupivacaine HCl) injection Recalled by Hospira Inc., A Pfizer...
The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass RX Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides...
The Issue: The firm sent the Technical Bulletin to consignees who received the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.