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. 2,724 recalls have been distributed to Washington in the last 12 months.
Showing 18601–18620 of 51,768 recalls
Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...
The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium 10 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl
The Issue: Cross Contamination with Other Product(s): containers labeled as having...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 2 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl
The Issue: Cross Contamination with Other Product(s): containers labeled as having...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl
The Issue: Cross Contamination with Other Product(s): containers labeled as having...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl
The Issue: Cross Contamination with Other Product(s): containers labeled as having...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Subpotent Drug:...
The Issue: Subpotent Drug: Out-of-Specification potency results at the 30-day stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.