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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 26121–26140 of 27,462 recalls
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed EL Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...
The Issue: GE Healthcare became aware of a potential issue associated with the LOGIQ e...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Information Center/Client and Philips IntelliVue...
The Issue: Internal audio cable may have diminished retention force due to damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses...
The Issue: The lenses exceeded the acceptance limit for silicone oil residual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnteraLite Infinity Enteral Feeding Pump identified with the following list...
The Issue: MOOG Medical Devices Group is conducting a voluntary for a limited set of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Angio Drape Pack Radiology-LF Recalled by Medline Industries Inc Due...
The Issue: The non-sterile Waste Bag component in the custom pack was attached to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.