replacement available Recalls

280 recalls tagged with “replacement available”.

Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 7 M12 Recall 2026 for Intermittent X-ray Imaging in 1994 Units

Philips recalled 1,994 Azurion 7 M12 interventional X-ray systems, including 360 units in the United States, for a wiring-foot switch defect that may fail to initiate imaging. The issue can cause imaging to not start or operate intermittently. Hospitals and clinicians should stop using affected devices immediately and follow the manufacturer’s recall instructions.

Philips
Philips has
Read more
Health & Personal Care
HIGH
FDA DRUG

ARTIFICIAL TEARS Dry Eye Relief Eye Drops Recalled in 2026 Over Sterility Concerns

More than 1.02 million bottles of Dry Eye Relief Eye Drops across multiple brands were recalled nationwide on March 3, 2026. The products were distributed by KC Pharmaceuticals and sold at retailers including Rite Aid, Meijer and H-E-B. The FDA notice cites a lack of assurance of sterility as the reason for the recall. Stop using these products immediately and contact KC Pharmaceuticals for next‑s

ARTIFICIAL TEARS
Lack of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 7 M20 X-ray System Recall Affects 5,167 Units Worldwide (2026)

Philips Medical Systems Nederland recalled 5,167 Azurion 7 M20 X-ray imaging systems sold to healthcare facilities in the U.S. and internationally. The wired foot switch can fail to initiate imaging or produce intermittent imaging. Hospitals and clinics should stop using the device and follow recall instructions from Philips, with notification by letter to affected parties.

Philips Medical Systems Nederland
Philips has
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD10F Recall for 10 Units Worldwide (2026)

Philips Medical Systems Nederland B.V. recalls 10 Allura Xper FD10F imaging systems sold to hospitals worldwide. The devices may fail to start X-ray imaging or start intermittently when using the wired foot switch. Hospitals should stop using the devices immediately and contact Philips for instructions.

Philips Medical Systems Nederland B.V.
Philips has
Read more
Health & Personal Care
HIGH
FDA DRUG

KC Pharmaceuticals Sterile Eye Drops Soothing Tears Recall 74,016 Bottles (2026)

KC Pharmaceuticals recalls 74,016 bottles of Sterile Eye Drops Soothing Tears distributed nationwide by Rugby Laboratories and Walgreens. The recall cites a lack of assurance of sterility. Consumers and healthcare providers should stop using the product immediately and contact KC Pharmaceuticals for guidance.

KC Pharmaceuticals
Lack of
Read more
Food & Beverages
HIGH
FDA FOOD

Ajinomoto Tai Pei Shrimp Fried Rice Recalled for Glass Shards in 9,913 Cases (2026)

Ajinomoto Foods North America recalled 9,913 cases distributed nationwide after glass fragments were found in Tai Pei Shrimp Fried Rice. The glass pieces measure 1-3 cm long and 2-4 mm wide. Consumers should not eat the product and should contact Ajinomoto for refund or replacement information.

Ajinomoto Foods North America
Foreign objects
Read more
Food & Beverages
HIGH
FDA FOOD

Ajinomoto Golden Tiger Vegetable Fried Rice Recalled for Glass Contamination (2026)

Ajinomoto Foods North America recalls Ajinomoto Golden Tiger Vegetable Fried Rice sold at multiple retailers nationwide. Glass fragments measuring 1-3 cm long and 2-4 mm wide have been found in frozen rice. Consumers should not eat the product and should contact Ajinomoto for refunds or replacements.

Ajinomoto Foods North America
Foreign objects
Read more
Food & Beverages
HIGH
FDA FOOD

Ajinomoto Ling Ling Restaurant Style Fried Rice Recall: 3,780 Cases Glass Fragments (2026)

Ajinomoto Foods North America recalled 24,796 pounds of Ling Ling Restaurant Style Fried Rice Savory Vegetable sold in multiple states. Glass fragments were found in the product and measure 1–3 cm long and 2–4 mm wide. Consumers should not eat the product and should contact Ajinomoto Foods North America for a refund or replacement.

Ajinomoto Foods North America
Foreign objects
Read more
Food & Beverages
HIGH
FDA FOOD

Ajinomoto Vegetable Gyoza Dumplings 12ct Recalled for Glass Shards (2026)

Ajinomoto Foods North America recalled 8,097 cases of Ajinomoto Vegetable Gyoza Dumplings sold nationwide through retailers. Glass fragments measuring 1 to 3 cm long and 2 to 4 mm wide were found in the product. Consumers should not eat the dumplings and should contact Ajinomoto Foods North America for refund or replacement.

Ajinomoto Foods North America
Foreign objects
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/20 OR Table Recalled for Intermittent X-ray Activation (2026)

Philips Medical Systems Nederland B.V. recalled 5 Allura Xper FD20/20 OR Tables distributed nationwide and internationally after detecting intermittent X-ray activation with the wired foot switch. The defect can prevent X-ray imaging from starting or cause it to stop during procedures. Hospitals and clinicians should stop using the affected tables and await manufacturer guidance.

Philips Medical Systems Nederland
Philips has
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Biplane Recalled for Intermittent X-Ray Imaging (2026)

Philips Medical Systems Nederland B.V. recalled 461 Allura Xper FD20 Biplanes sold to healthcare facilities nationwide and internationally. X-ray imaging may not initiate or may occur intermittently when using the wired foot switch. Hospitals should stop using the devices immediately and follow Philips’ recall instructions.

Philips
Philips has
Read more
Health & Personal Care
HIGH
FDA DRUG

Rising Pharmaceuticals Temozolomide 5 mg Capsules Recall 1,200 Bottles in 2026

Rising Pharmaceuticals recalls 1,200 Temozolomide 5 mg capsules nationwide after a stability test found out-of-spec impurities. The drug is Rx-only, with NDC 16571-816-51 and lot 1TM0524003A. Stop using immediately and contact a healthcare provider for guidance.

Rising Pharmaceuticals
Failed Impurities/Degradation
Read more
Food & Beverages
HIGH
FDA FOOD

Ajinomoto Foods North America Recalls 35,955 Pounds of Japanese-Style Fried Rice for Glass Contamin‑

Ajinomoto Foods North America recalled 35,955 pounds of Ajinomoto Japanese-Style Vegetable Fried Rice distributed by multiple retailers in 43 states after glass fragments were found in the product. The glass pieces measure 1 to 3 cm long and 2 to 4 mm wide. Consumers who bought the product should not eat it and should contact Ajinomoto Foods North America for a refund or replacement.

Ajinomoto Foods North America
Foreign objects
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

Civco Medical eTRAX 14G Needle Sensor Recall for 5 Units (2026)

Civco Medical Instruments Co. is recalling 5 eTRAX Needle Sensor 14G units for Aurora Trackers. The recall cites a programming and inspection error that could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.

Civco Medical Instruments Co.
There was
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

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 2 eTRAX 12G Starter Kits for Aurora Trackers (2026)

Civco Medical Instruments recalled 2 eTRAX Needle System Starter Kit 12G units for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The defect can cause the needle tip position to be incorrectly identified on the user interface. Stop using the device immediately and follow the recall instructions from Civco or your healthcare provider.

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
Previous
12345...14
Next

Tag Statistics

Total Recalls
280

Related Tags

electrical hazardimmediate actionstop use immediatelyfda regulatedcpsc regulatedchemical hazardreturn for refundinfant productadult productelderly productkitchenbathroom