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. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 23341–23360 of 48,219 recalls
Recalled Item: Lipo MIC-12 Compound Injectable a) NDC 69699-1603-10 Recalled by Pharm D...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trimix ST-1 30PA-1.5PH-50A Aqueous Solution Pharm D Solutions Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...
The Issue: Potential for outer pouch sterile barrier to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISIONIST X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...
The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME)...
The Issue: Firm identified an issue in the manufacturing process which might contribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...
The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...
The Issue: The action is being initiated because the cooling indicator board was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codan Filter (Codan catalog number BC 693) used with Medrad Recalled by...
The Issue: Bayer has received reports of loose particulate in the filter when the dust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Delivers 0.1 mg/day...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole dihydrochloride extended release tablets Recalled by Par...
The Issue: Failed impurities/degradation specifications: Finished product contain a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.