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. 2,572 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,572 in last 12 months

Showing 4086140880 of 51,768 recalls

DrugMarch 10, 2015· the Compounder

Recalled Item: ESTRIOL (E3) W/V (weight/volume) VERSABASE 3MG/ML Transdermal cream Recalled...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: ESTRIOL (E3) 2.5MG suppositories Recalled by the Compounder Due to Recalled...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· US Endoscopy Group Inc

Recalled Item: Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire...

The Issue: A wire component on the distal grasping assembly of the device became detached..

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) MOTOR MODULE Recalled by Microtek Medical Inc Due to This...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE Recalled by Microtek Medical Inc Due...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NOBELREPLACE Tapered Groovy RP 4.3x10mm Recalled by Nobel Biocare Usa Llc...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: HTM Mechanism Set Set 16 Recalled by Specialty Appliance Works, Inc. Due to...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 Recalled by Specialty...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: MiniScope Hst ROC Crown 15 Patient Kit Recalled by Specialty Appliance...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing