Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,431 recalls have been distributed to Oklahoma in the last 12 months.
Showing 40241–40260 of 49,976 recalls
Recalled Item: ACCU-CHEK Tender II 17/110 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 13/80 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended Recalled...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 13/110 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia 1000 Instrument (introduced as UniCAP 1000) Recalled by Phadia US Inc...
The Issue: During an investigation of instrument logs it was determined that In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaMap Orion High Resolution Mapping Catheter Recalled by Boston...
The Issue: Some IntellaMap Orion High Resolution Mapping Catheters are exhibiting a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GINSENG KIANPI PIL Recalled by One and Zen Due to Undeclared Dexamethasone
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wake-Up Instant Coffee Mix (weasel coffee) Melange de Cafe Instantane...
The Issue: Firm was notified by CFIA and FDA that CFIA testing found undeclared milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mercaptopurine Tablets Recalled by American Health Packaging Due to Failed...
The Issue: Failed USP Dissolution Test Requirements: This sub-recall is in response to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models:M3535A Recalled by...
The Issue: MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECG Out Cable Recalled by Philips Electronics North America Corporation Due...
The Issue: When a Philips monitor/defibrillator is receiving an ECG signal from an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A...
The Issue: 1. Device will perform the weekly automated tests hourly, which could cause...
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 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.