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. 1,067 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,067 in last 12 months

Showing 17281–17300 of 53,829 recalls

Medical DeviceMarch 22, 2021· QURA S.R.L.

Recalled Item: Spectrum Medical Quantum Standard heat exchanger Recalled by QURA S.R.L. Due...

The Issue: Product labeled as sterile may not have been adequately sterilized. In...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica CEMIX Recalled by BIOPSYBELL S.R.L. Due to Products labeled as...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP Recalled...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 8G DIRECT WORKING CANNULA BEVEL TIP Recalled by BIOPSYBELL S.R.L. Due to...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10G DIRECT WORKING CANNULA BEVEL TIP 15CM Recalled by BIOPSYBELL S.R.L. Due...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT Recalled by...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· Datascope Corp.

Recalled Item: Cardiosave Rescue IABP - Product Usage: used to inflate and Recalled by...

The Issue: There are cybersecurity vulnerabilities in a widely used low-level TCP/IP...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT SINGLE - ACCESS Recalled by BIOPSYBELL S.R.L. Due to Products...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10G COAXIAL CANNULA WITH TUOHY CONNECTION Recalled by BIOPSYBELL S.R.L. Due...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) Recalled by BIOPSYBELL...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· Normand-Info S.A.S.U.

Recalled Item: Normand Remisol Advance Data Manager is a software device that Recalled by...

The Issue: Instructions For Use for software versions 1.5 to 1.9 did not provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10 GAUGE DRILL Recalled by BIOPSYBELL S.R.L. Due to Products labeled as...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: CEMENT MIXING SYSTEM Recalled by BIOPSYBELL S.R.L. Due to Products labeled...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp PenFill (insulin aspart injection) 100 units/mL (U-100) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Xultophy 100/3.6 (insulin degludec and liraglutide injection) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Levemir FlexTouch (insulin detemir) injection Recalled by Novo Nordisk Inc...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp (insulin aspart injection) Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp FlexTouch (insulin aspart injection) 100 units/mL (U-100) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA FlexTouch (insulin degludec injection) 100 units/mL (U-100) Recalled...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund