Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,813 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,813 in last 12 months

Showing 65416560 of 53,829 recalls

Medical DeviceMarch 18, 2024· Angiodynamics, Inc.

Recalled Item: DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK Recalled by Angiodynamics, Inc....

The Issue: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· Angiodynamics, Inc.

Recalled Item: DURAMAX STACKED TIP 32 CM STRAIGHT VASC-PAK Recalled by Angiodynamics, Inc....

The Issue: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· Angiodynamics, Inc.

Recalled Item: DURAFLOW 2 Recalled by Angiodynamics, Inc. Due to Tri-Ball Tunneler may...

The Issue: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· Angiodynamics, Inc.

Recalled Item: DURAFLOW 2 Recalled by Angiodynamics, Inc. Due to Tri-Ball Tunneler may...

The Issue: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Innova IGS 5 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 7 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· Angiodynamics, Inc.

Recalled Item: DURAFLOW 2 Recalled by Angiodynamics, Inc. Due to Tri-Ball Tunneler may...

The Issue: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Innova IGS 6 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· Angiodynamics, Inc.

Recalled Item: DURAMAX STACKED TIP 24CM STR. BASIC KIT Recalled by Angiodynamics, Inc. Due...

The Issue: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· Angiodynamics, Inc.

Recalled Item: DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK Recalled by Angiodynamics, Inc....

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· XENEX Disinfection Services Inc.

Recalled Item: LightStrike Blackout Curtains Recalled by XENEX Disinfection Services Inc....

The Issue: Blackout curtains are no longer recommended as a protective barrier against...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· SPINEART SA

Recalled Item: PERLA TL 25D SCREW 45 25-S TLF-DS 45 Recalled by SPINEART SA Due to Due to...

The Issue: Due to receiving information regarding difficulties with the insertion of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Seprafilm Adhesion Barrier 1 Half Sheet Recalled by Baxter Healthcare...

The Issue: Product was distributed in the United States without proper regulatory approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· Covidien LP

Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm)...

The Issue: Products may not be heparin coated as indicated on the label-leads to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· Alcon Research, LLC

Recalled Item: Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga...

The Issue: Due to complaints of particulates, residue, occlusions, and bent tips for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· Covidien LP

Recalled Item: Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x Recalled by...

The Issue: Products may not be heparin coated as indicated on the label-leads to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile convenience kits: a. Medline Retrograde PK-22025203-LF Recalled by...

The Issue: Surgical convenience kits containing Pure Pouch component that has weak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Non-sterile convenience kits: a. Medline Difficult Airway Tray W/O Cook...

The Issue: Surgical convenience kits containing Pure Pouch component that has weak...

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

Class II — Potential Health HazardOngoing