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. 949 recalls have been distributed to Arkansas in the last 12 months.
Showing 40361–40380 of 49,990 recalls
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: Device may malfunction, which could cause therapy to be delayed, disabled,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx...
The Issue: KCI has received reports that, in a small number of cases, the CelluTome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and...
The Issue: HORIBA Medical is informing all HORIBA Medical Lite DM customers using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product comes in as part of Fabulous Fudge Gift Box. Recalled by Tastefully...
The Issue: Tastefully Simple is recalling various lots of Cookie & Cream Fudge(Fabulous...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lemoncello Mascarpone Cake Recalled by Cheesecake Royale, Inc. Due to...
The Issue: Recalled product contains undeclared FD&C Yellow #5 and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Turtle Fudge Brownies Recalled by Cheesecake Royale, Inc. Due to Undeclared...
The Issue: Recalled product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rocky Road Brownies Recalled by Cheesecake Royale, Inc. Due to Undeclared Wheat
The Issue: Recalled product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CARROT CAKE Recalled by Cheesecake Royale, Inc. Due to Undeclared Walnuts
The Issue: Recalled product contains undeclared walnuts. Walnut is not listed on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.