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. 2,367 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,367 in last 12 months

Showing 2734127360 of 48,219 recalls

Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt HV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Spectra-System/Legacy Guided Surgery Handle Kit Recalled by Implant Direct...

The Issue: The inside diameter of the 2.3mm small drill guide inserts have a smaller...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 15 mMol in Recalled by...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in Recalled by...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Succinylcholine Chloride Injection (Preserved) 20 mg per mL Recalled by...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Latanoprost PF Solution Recalled by ImprimisRx CA, Inc., dba ImprimisRx Due...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Curcumin Emulsion 10mg/ml Injection Recalled by ImprimisRx CA, Inc., dba...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Timolol-Latanoprost PF Solution (0.5-0.005)% Recalled by ImprimisRx CA,...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing