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. 1,020 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,020 in last 12 months

Showing 15341–15360 of 48,219 recalls

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: EASYNJECT Recalled by BIOPSYBELL S.R.L. Due to Products labeled as sterile...

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: 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: 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· Datascope Corp.

Recalled Item: Cardiosave Hybrid 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: 10G 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: RENOVA SPINE BONE FILLER 10G 12CM CENTIM. STERILE 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· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT WORKING CANNULA DIAMOND TIP MINI Recalled by BIOPSYBELL S.R.L....

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· 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: 10 GAUGE SINGLE CEMENT 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· 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: 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
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
FoodMarch 22, 2021· Simply Delicious Inc.

Recalled Item: Bobo's Maple Pecan Oat Bars Recalled by Simply Delicious Inc. Due to Two...

The Issue: Two consumer complaints were received for peanuts in maple pecan bars.

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

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: TRESIBA (insulin degludec injection) 100 units/mL (U-100) Recalled by Novo...

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) 200 units/mL (U-200) 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
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: NovoLog (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