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. 2,433 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,433 in last 12 months

Showing 4920149220 of 51,768 recalls

Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For...

The Issue: The microelectrodes are not flush with the silastic substrate, may contain...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...

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

Class II — Potential Health HazardOngoing
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond Pill Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond PLATINUM Capsules Recalled by Performance Plus Marketing, Inc....

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: CASANOVA Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights SUPREME Capsules Recalled by Performance Plus Marketing, Inc....

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow XXXTREME Capsules Recalled by Performance Plus Marketing, Inc. Due...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL (bupivacaine liposome injectable suspension) Recalled by Pacira...

The Issue: Subpotent; bupivacaine

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· L. Perrigo Co.

Recalled Item: Prednisone tablets Recalled by L. Perrigo Co. Due to Presence of Foreign...

The Issue: Presence of Foreign Substance(s); Perrigo has been notified of a recall by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 17, 2012· Animas Corporation

Recalled Item: Animas(R) 2020 Recalled by Animas Corporation Due to Due to an internal...

The Issue: Due to an internal calendar date limit (December 31, 2015) these pumps will...

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

Class III — Low RiskOngoing
Medical DeviceDecember 17, 2012· Mizuho OSI

Recalled Item: Mizuho Orthopedic Table Recalled by Mizuho OSI Due to Possible instability...

The Issue: Possible instability of Orthopedic Table Top. If the epoxy bond fails, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2012· Medacta Usa Inc

Recalled Item: Medacta Quadra Trial Broach size 0 part # 01.10.10.045 Recalled by Medacta...

The Issue: The tip of the Quadra Trial Broach size 0, broke during a surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2012· Intel-GE Care Innovations LLC

Recalled Item: QuietCare-Networked product Recalled by Intel-GE Care Innovations LLC Due to...

The Issue: Care Innovations detected a software anomaly: During the engineering...

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

Class II — Potential Health HazardOngoing
DrugDecember 14, 2012· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Mylan...

The Issue: Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 13, 2012· Watson Laboratories Inc

Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...

The Issue: Impurities/Degradation Products: Out-of-specification results were obtained...

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

Class III — Low RiskOngoing
Refund
FoodDecember 13, 2012· Ocean Beauty Seafoods, LLC

Recalled Item: Cold-smoked salmon in vacuum plastic bags that are partially clear Recalled...

The Issue: Ocean Beauty Seafood's sample was found positive for Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund