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. 2,590 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,590 in last 12 months

Showing 1386113880 of 28,355 recalls

Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: TRIPLE LUMEN BUNDLE KIT ECVC1540 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: INFUSA PORT KIT DYNDC1840F Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: UVC TRAY UVT875 Recalled by Centurion Medical Products Corporation Due to...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: IV START KIT IV8440 Recalled by Centurion Medical Products Corporation Due...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: VANTEX 7FR Recalled by Centurion Medical Products Corporation Due to Firm...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PORT AND IO ACCESS DRESSING KIT DT15780A Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CENTRAL LINE BUNDLE ECVC6375 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: IV KIT - SORBAVIEW IVS3475 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CAP BUNDLE KIT DYNDC2137 Recalled by Centurion Medical Products Corporation...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840 Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Stryker Corporation

Recalled Item: Stryker Connected OR Cart Recalled by Stryker Corporation Due to There is a...

The Issue: There is a potential problem with firm s Connected OR Cart, 120V resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45041 HPK1A...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code:JR 42563 HPHNM Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC Kit Product Code: ASK 45541 LVH1 Recalled by Arrow International...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Precision Integrated System 120V Recalled by CooperSurgical, Inc. Due...

The Issue: 2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator...

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

Class II — Potential Health HazardOngoing