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. 1,751 recalls have been distributed to Wyoming in the last 12 months.
Showing 40121–40140 of 48,219 recalls
Recalled Item: Humidifier Adaptor 040 Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a...
The Issue: In the case of a loss of GUI display due to a Backlight Inverter PCBA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALL Medical Breathing Circuit Filter Recalled by Pall Corporation Due to...
The Issue: Possible leak from the filter allowing a small of amount of air to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch Critical Care Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has received complaints from the field alleging instances where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ferrous Gluconate Tablets Recalled by National Vitamin Co Inc Due to Mislabeling
The Issue: National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROSA Surgical Device 2.5.8 It is intended to be used Recalled by Zimmer...
The Issue: Software corrections reactivating the cooperative endoscopy mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eye-pak 7407 Tray Support Cover Recalled by Alcon Research, Ltd. Due to The...
The Issue: The peel pouches of the Tray Support Covers may be insufficiently sealed so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 300 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System...
The Issue: Covidien is conducting a medical device field correction for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use Recalled...
The Issue: Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Recalled by...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus...
The Issue: Springs contained in the access door hinge assembly on the Walk Away Plus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.