Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,142 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,142 in last 12 months

Showing 13981–14000 of 55,713 recalls

DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Product: Product is contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 3, 2022· Intuitive Surgical, Inc.

Recalled Item: VESSEL SEALER EXTEND Recalled by Intuitive Surgical, Inc. Due to Placing...

The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Intuitive Surgical, Inc.

Recalled Item: DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi' Recalled by Intuitive...

The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Boston Scientific Corporation

Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 1) UPN: M00542420 Recalled by...

The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Boston Scientific Corporation

Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 1) UPN:M0054242CE0 Intended Use:...

The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled...

The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled by...

The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Boston Scientific Corporation

Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended...

The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled by...

The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled...

The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...

The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...

The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2022· Boston Scientific Corporation

Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 2) UPN: M00542421 Recalled by...

The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2022· ASO LLC

Recalled Item: First Aid Kits containing acetaminophen under brand names Equate (Walmart)...

The Issue: Kits contained recalled acetaminophen.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2022· Medtronic Inc

Recalled Item: Harmony Delivery Catheter System. Part of the Harmony Transcatheter...

The Issue: There is potential for the capsule bond to break during the procedure.

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

Class I — Serious Health HazardOngoing