Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,020 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,020 in last 12 months

Showing 15401–15420 of 48,219 recalls

Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar Recalled by Becton Dickinson & Co. Due to Products...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Clark Laboratories, Inc.

Recalled Item: Trinity Biotech Captia Measles IgM Kit Recalled by Clark Laboratories, Inc....

The Issue: Positive Control may run high out of its assigned ISR range and result in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· SIGHT DIAGNOSTICS LTD

Recalled Item: Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #:...

The Issue: Discrepancy in labeling between the adult CBC ranges presented in the OLO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Medtronic Sofamor Danek USA, Inc

Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...

The Issue: The shelf box identifies a small device actually contains a large device,...

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

Class II — Potential Health HazardOngoing
FoodMarch 17, 2021· Real Water, Inc.

Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...

The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 17, 2021· Real Water, Inc.

Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...

The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 17, 2021· Alembic Pharmaceuticals Limited

Recalled Item: Telmisartan Tablets Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Labeling: Label-mixup

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Biomerieux Inc

Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...

The Issue: bioMerieux received complaints about calibration issue observed on several...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LANCETS 28G 100CT Item Number:2975670 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033 Recalled by Cardinal...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: BD UF PEN 32GX4MM 100 NANO Item Number: 4292272 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port Recalled by...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 60mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.3 mL Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing