Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,535 in last 12 months

Showing 1722117240 of 28,355 recalls

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 DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 105" (267 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: 107" (272 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: 120" (305 cm) 10 Drop Primary Set w/2 MicroClave¿ 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: 218 cm (86") Appx 16.4 ml Recalled by ICU Medical, Inc. Due to Some devices...

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: 88" (224 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: 140" (356 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: 139" (353 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" Y-Type Blood Set w/170 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: 94" (239 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: 94" (239 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· Cook Inc.

Recalled Item: Central Venous Catheter Set Triple Lumen Polyurethane Recalled by Cook Inc....

The Issue: Central venous catheters may not fit over guide wire potentially causing...

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

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

Recalled Item: Central Venous Catheter Tray Triple Lumen Polyurethane Recalled by Cook Inc....

The Issue: Central venous catheters may not fit over guide wire potentially causing...

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: 132" (335 cm) Y-Type Admin 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
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· Cook Inc.

Recalled Item: Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane...

The Issue: Central venous catheters may not fit over guide wire potentially causing...

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: 132" (335 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: 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