Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,092 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,092 in last 12 months

Showing 16681–16700 of 51,768 recalls

Medical DeviceMarch 25, 2021· Zavation

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

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2021· Cosette Pharmaceuticals, Inc.

Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...

The Issue: CGMP Deviaitons

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· S & B Story LLC

Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· Namoo Enterprise LLC

Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Moisture Limits: Out of specification for water content

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2021· Bit & Bet LLC

Recalled Item: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2021· Becton Dickinson & Co.

Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...

The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2021· Pacific Medical Group Inc.

Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...

The Issue: Aftermarket front bezel components were installed during service/repair, not...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 24, 2021· Gf Health Products

Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...

The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2021· Medtronic Inc.

Recalled Item: VenaSeal Closure System Recalled by Medtronic Inc. Due to Firm received...

The Issue: Firm received increased number of reports that VenaSeal dispensing systems...

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· 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: 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· 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: 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· 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