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. 1,932 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,932 in last 12 months

Showing 2234122360 of 53,829 recalls

Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a / 980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2019· West-Ward Columbus Inc

Recalled Item: Oxcarbazepine Oral Suspension Recalled by West-Ward Columbus Inc Due to...

The Issue: Failed Impurities/Degradation Specificattion

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Darmerica, LLC

Recalled Item: Quinacrine Dihydrochloride (98.25%) Recalled by Darmerica, LLC Due to Label...

The Issue: Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 6, 2019· Cardinal Health dba Specialty Pharmaceutical Services

Recalled Item: Nucala (mepolizumab) Injection Recalled by Cardinal Health dba Specialty...

The Issue: Temperature Abuse; Product stored and shipped outside of labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Torrent Pharma Inc.

Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High Out Of Specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Mylan Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications:OOS for unknown impurity.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 6, 2019· Pfizer Inc.

Recalled Item: Bacteriostatic Water for Injection Recalled by Pfizer Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 6, 2019· ConAgra Foods, INc.

Recalled Item: Udi's Classic Hamburger Buns Recalled by ConAgra Foods, INc. Due to Foreign...

The Issue: potential presence of foreign material

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 6, 2019· Medline Industries Inc

Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...

The Issue: The recall is being conducted due to a potential defective component on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2019· CooperSurgical, Inc.

Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...

The Issue: The touchpad may not work properly after cleaning.

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

Class III — Low RiskOngoing
FoodSeptember 4, 2019· McCain Foods USA

Recalled Item: Ore Ida Spud Bites Recalled by McCain Foods USA Due to Foreign Object...

The Issue: presence of hard foreign material

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: Synchron Systems Opiate 2000 ng Reagent (OP2 1 x 250) Recalled by Beckman...

The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: Opiate 300 Ng Reagent (OP 1 X 250) for use Recalled by Beckman Coulter Inc....

The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate 300...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Elekta Inc

Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...

The Issue: It is possible that the forced electron density settings will be changed for...

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

Class II — Potential Health HazardOngoing