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. 2,612 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,612 in last 12 months

Showing 2952129540 of 51,768 recalls

FoodAugust 2, 2017· Amrita Health Foods

Recalled Item: Amrita Apple Cinnamon Energy Bar Recalled by Amrita Health Foods Due to...

The Issue: Product may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Major Poly-Vita Drops with Iron Recalled by The Harvard Drug Group Due to...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· Amrita Health Foods

Recalled Item: Amrita Pineapple Chia Energy Bar Recalled by Amrita Health Foods Due to...

The Issue: Product may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 1, 2017· The Ampt Life, LLC

Recalled Item: NATURAL HERBAL COFFEE AMPT Recalled by The Ampt Life, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 1, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Segmental System Recalled by Zimmer Biomet, Inc. Due to The products...

The Issue: The products being recalled exceeded the weight previously tested leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2017· Zimmer Biomet, Inc.

Recalled Item: Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled Recalled by...

The Issue: The products being recalled exceeded the weight previously tested leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2017· Cardinal Health 200, LLC

Recalled Item: Presource(R) Kits (custom surgical/procedural kits): The standard and custom...

The Issue: The firm manufactured and distributed Presource(R) kits which contained BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 121" (307 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 115" (292 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 99" (251 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 99" (251 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 112" (284 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 108" 20 Drop Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 116" (295 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 185 cm (73") Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 85" (216 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 80" (203 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 84" (213 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 137" (348 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 175" (445 cm) Y-Type Blood Set w/170 Micron Blood Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing