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. 2,342 recalls have been distributed to Wyoming in the last 12 months.
Showing 35261–35280 of 48,219 recalls
Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...
The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...
The Issue: A software fix has been released to prevent automatic movement resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling
The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...
The Issue: Unexpected rate of postoperative fractures resulting in the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angiographic Injector. Medrad Mark 7 Arterion Injection System Recalled by...
The Issue: Software Version SW 005.006_SH, resulted in the removal of purge enforcement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap...
The Issue: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rivastigmine Tartrate Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Concentrated coffee packed in 1/2 gallon or 1 gallon hermetically Recalled...
The Issue: The pH level in coffee product was elevated above 4.6.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ferno iNX Wheeled Stretcher Recalled by Ferno-Washington Inc Due to Hole...
The Issue: Hole elongation in the telescoping load frame channel. A hole elongation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer....
The Issue: Flow restriction issues in a trifurcated IV set included in the pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: Recalled...
The Issue: Potential to improperly characterize tissue within the jaws, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Recalled...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Argyle Infant Heel Warmers (no tab) Item Code: MH00002N Recalled by...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.