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.
Showing 40981–41000 of 51,768 recalls
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Brilliance Workstation (Uninterruptible Power Supply (UPS)...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALL ASN products: The ASN products are in capsule or Recalled by James G....
The Issue: All ASN brand products are recalled because it was ordered by the United...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ALL MAXAM PRODUCTS: The Maxam product is used orally in Recalled by James G....
The Issue: All Maxam brand products are recalled because it was ordered by the United...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION Recalled by Hospira Inc. Due to...
The Issue: Labeling: Wrong Bar Code: There is a potential for some units to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% DEXTROSE Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: there is a potential for solution to leak at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed finding of human hair floating in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product...
The Issue: A potential issue was detected that could result in blood leakage from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium VG Recalled by GE Healthcare Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique...
The Issue: The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD...
The Issue: A potential issue was detected that could result in blood leakage from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN 3000 Series Set- Huber needles. Used in combination Recalled by...
The Issue: Needle is leaking from hub/needle cannula connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. Recalled by Merge Healthcare, Inc. Due to There is a...
The Issue: There is a potential for duplicate container numbers to be created for patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LP Rotate Foot System prosthetic device for fitting lower extremity Recalled...
The Issue: The threads of the outer tube of the shock module of LP Rotate are too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS Femoral Implants Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An issue with photon dose calculation for DMLC (Dynamic MLC) plans for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamondback 360 Coronary Orbital Atherectomy System Recalled by...
The Issue: The OAD saline sheath outer layer may flake off from the catheter due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics cat no. G327 HardyCHROM SS Agar (HardyCHROM Salmonella...
The Issue: The firm is recalling HardyCHROM SS, Cat. no. G327 Lot no. 15037 due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.