replacement available Recalls

1,215 recalls tagged with “replacement available”.

Health & Personal Care
HIGH
FDA DEVICE

Civco Medical Instruments Recalls 21 eTRAX Needle Sensors for Aurora Trackers (2026)

Civco Medical Instruments Co. recalled 21 eTRAX Needle Sensors for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The devices have an inspection and programming error that can cause the needle tip position to be misidentified on the user interface. Clinicians should stop using the devices immediately and follow recall instructions from Civco.

Civco Medical Instruments Co.
There was
Read more
Health & Personal Care
HIGH
FDA DEVICE

Civco Medical Instruments Recalls 20 eTRAX Needle System Starter Kit 18G for Aurora Trackers (2026)

Civco Medical Instruments recalled 20 eTRAX Needle System Starter Kit 18G for Aurora Trackers. An error in inspection and programming of the needle sensor can cause needle tip position to be misidentified on the user interface. Healthcare providers and facilities should stop using the device immediately and follow the recall instructions from the manufacturer.

Civco Medical Instruments
There was
Read more
Health & Personal Care
CRITICAL
FDA DEVICE

Philips Respironics Trilogy Evo O2 Ventilator Recall Affects 113,717 Units in 2026

Philips Respironics recalls 113,717 Trilogy Evo O2 home-use ventilators in 2026. The Obstruction Alarm may fail to trigger within required standards, delaying warning for airway obstruction for up to four breaths. Stop using the device and follow recall instructions from Philips or your clinician.

Philips Respironics
In some
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy Evo Ventilator Recall 2026 Affects 113,717 Units

Philips Respironics recalled 113,717 Trilogy Evo home-use ventilators worldwide after finding the Obstruction Alarm may fail to trigger, potentially delaying alerts by up to four breaths. The devices were distributed nationwide in the United States and internationally. Consumers should stop using the device immediately and follow the manufacturer’s recall instructions.

Philips Respironics
In some
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy Evo Universal Ventilator Recall 113,717 Units (2026)

Philips Respironics recalled 113,717 Trilogy Evo Universal home-use ventilators sold by multiple retailers after alarms may fail to trigger. The obstruction alarm may not trigger within the required timeframe, delaying warning by up to four breaths. Patients should stop using the device and follow the manufacturer’s recall instructions or contact their healthcare provider for guidance.

Philips Respironics
In some
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy EV300 Recalled 113,717 Units Worldwide for Tidal Volume Discrepancy (202

Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold worldwide through healthcare distributors on March 2, 2026. Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may cause a mismatch between the set tidal volume and the delivered tidal volume. Patients and healthcare providers should stop using the device immediately and follow the recall instructions from the 제조

Philips Respironics
Using non-pneumatic
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy EV300 Ventilator Recall Affects 113,717 Units in 2026

Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold in the United States and internationally after determining the Obstruction Alarm may fail to trigger within required standards. The alarm can delay alerting caregivers for up to four breaths. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Philips or their clinician.

Philips Respironics
In some
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Angiography Kit Recall: 3,120 Medical Convenience Kits With NAMIC Adaptor May Disconnect (Z-

Medline Industries, LP recalls 3,120 medical convenience kits worldwide due to a risk the syringe rotating adaptor may unwind during use. The issue can create a loose connection or complete disconnection between the syringe and manifold. The recall was issued on February 27, 2026 and is active. Customers should stop using the kit and follow manufacturer instructions for recall notices.

Medline Industries, LP
Medline Industries,
Read more
Food & Beverages
HIGH
FDA FOOD

Savannah Bee Company Honey BBQ Sauce Mustard Recalled for Soy and Wheat Allergens (2026)

4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.

Savannah Bee Company
Undeclared Allergens:
Read more
Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare SIGNA Premier MRI Systems Recalled Worldwide for Ferrous Fittings Hazard (41 Units, 6)

GE Healthcare recalled 41 SIGNA Premier Whole-Body MRI systems sold worldwide. The devices may have ferrous fittings on the magnet rear instead of brass. If service is performed while the magnet is ramped, the magnetic field could attract the fittings and injure personnel. Hospitals should stop using the devices and follow the manufacturer's recall instructions.

GE Healthcare
Whole-Body MR
Read more
Food & Beverages
HIGH
FDA FOOD

TG Foods Divided Sunset Multi Collagen Peptides 8 oz Recalled in 2026 Affects 7,980 Units

TG Foods recalled 7,980 units of Divided Sunset Multi Collagen Peptides 8 oz stand-up pouches distributed nationwide. The recall notes the ingredient statement lists wild caught marine collagen and eggshell membrane collagen but does not declare EGG or the specific fish species. Consumers should not consume the product and should contact TG Foods for refund or replacement information.

TG Foods
The product
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in Class I Action for 79,843 Units

Medline Industries issued a Class I recall for 79,843 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The action covers worldwide distribution including the US and PR. The risk is a syringe adaptor unwinding during use, which may cause a loose connection or disconnection with the manifold. Stop using the device immediately and follow recall instructions.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Spacelabs Healthcare 91496 Multi-parameter Module Recall Affects 1,790 Units Worldwide (2026)

Spacelabs Healthcare recalled the Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor, distributed worldwide. A circuit board issue in Auto mode may trigger CO readings improperly, causing Bad Curve or Irregular Curve errors. Stop using immediately and follow manufacturer instructions.

Spacelabs Healthcare
Multi-parameter command
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Syringe Recall Affects 17,902 Kits Worldwide (2026)

Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use immediately and follow recall instructions.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic RA Syringes Recalled in 1698 Kits for Unwinding Adaptor Risk (2026)

Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC RA Syringe Recall: 108 Units Worldwide for Unwinding Adaptor (High Risk)

Medline Industries, LP recalls 108 NAMIC Angiographic Rotating Adaptor Syringes sold worldwide, including the United States, PR and several international markets. The rotating adaptor may unwind during use, creating a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Adaptor Syringe Recall Expands Worldwide in 240 Kits (Class I)

Medline Industries, LP recalled 240 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers worldwide distribution including the US, Puerto Rico, and multiple international markets. The potential issue is the adaptor unwinding during use, risking a loose connection or disconnection with the manifold.

Medline Industries, LP
Medline Industries,
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in 82 Kits Worldwide

Medline Industries, LP recalled 82 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers two Medline SKUs and spans worldwide distribution, including the US, Puerto Rico and several countries. The defect is a rotating adaptor that may unwind, causing loose connections or disconnections between syringe and manifold.

Medline Industries, LP
Medline Industries,
Read more
Previous
12345...61
Next

Tag Statistics

Total Recalls
1,215

Related Tags

immediate actionstop use immediatelyfda regulatedcpsc regulatedelectronicmetalplasticbattery poweredoutdoorworkplaceadult productsummer product