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. 2,451 recalls have been distributed to Arkansas in the last 12 months.
Showing 26401–26420 of 28,355 recalls
Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...
The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...
The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Recalled by GE Healthcare, LLC Due to GE Healthcare has recently become...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...
The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...
The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin) Recalled...
The Issue: Use of affected lots may give false indication of susceptibility to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon Femoral Distal Augment- Left Recalled by...
The Issue: Stryker Orthopaedics received a report that a label on the external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Some of the KWIK-STIK...
The Issue: Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511...
The Issue: Medtronic is recalling the Medtronic Paradigm Insulin Pump because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Sterilization System Recalled by Advanced Sterilization...
The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC) Recalled by DePuy...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC)...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.