adult product Recalls

989 recalls tagged with “adult product”.

Health & Personal Care
HIGH
FDA DEVICE

BD 10 mL Luer-Lok Syringe Recalled Over Bundle Packaging Mix-Up in US; 204,000 Units Affected

BD recalled 204,000 10 mL Luer-Lok/Luer Slip syringes due to a packaging mix-up that placed Luer Slip syringes in a batch designated for Luer Lok syringes. The nationwide recall covers products distributed in California and Texas. Healthcare providers and patients should stop using the affected syringes immediately and consult manufacturer recall instructions.

Becton Dickinson
During the
Read more
Food & Beverages
HIGH
FDA FOOD

Khee Trading Recalls Frozen Oysters Due to Norovirus Risk

Khee Trading Inc. recalled 7,306 cases of Frozen Half Shell Oysters on January 27, 2026. The oysters may be contaminated with Norovirus, posing a serious health risk. Consumers should not consume the product and seek a refund or replacement.

Khee Trading
Imported oysters
Read more
Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella RP Recall 179 Units for Sensor Drift Risk (2026)

Abiomed recalled 179 Impella RP devices worldwide after a differential pressure sensor may drift. The fault can cause sensor values to drift, potentially affecting patient care. Stop using the device immediately and follow the recall instructions, including contacting Abiomed or your healthcare provider.

Abiomed
Differential pressure
Read more
Food & Beverages
HIGH
FDA FOOD

Beacon Promotions Recalls M&Ms Over Undeclared Allergens

Beacon Promotions recalled 5,788 units of repackaged M&Ms candies on January 26, 2026. The candies contain undeclared allergens, specifically milk, soy, and peanuts. Consumers should not consume these products and should seek refunds.

Beacon Promotions
Undeclared allergens
Read more
Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Estradiol Pellets Over Metal Contamination Risk

Asteria Health recalled 50,990 Estradiol pellets on January 26, 2026, due to potential metal particulate matter contamination. The recall affects products distributed nationwide in the USA. Consumers should stop using the pellets immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contaminants

Asteria Health recalled 4,599 testosterone pellets on January 26, 2026. The recall follows concerns over potential metal particulate matter contamination. Consumers should stop using the product immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Due to Contamination Risk

Asteria Health recalled 62,581 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. Consumers should stop using the product immediately and contact their healthcare provider for guidance. The recall affects testosterone pellets with specific lot numbers and expiration dates.

F.H. INVESTMENTS, Inc.
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contamination

Asteria Health recalled 153,498 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects lots expiring between June and September 2026. Consumers and healthcare providers must stop using the product immediately.

F.H. INVESTMENTS, Inc.
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contamination

Asteria Health recalled 194,336 testosterone pellets on January 26, 2026 due to potential metal contamination. Consumers must stop using the product immediately and contact their healthcare providers. The recall affects nationwide distribution in the USA.

F.H. INVESTMENTS, Inc.
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Due to Metal Contamination

Asteria Health recalled 1,758 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects pellets distributed nationwide in the USA. Consumers should stop using the product immediately and contact their healthcare providers for guidance.

F.H. INVESTMENTS, Inc.
Presence of
Read more
Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalled Testosterone Pellets Due to Metal Contamination

Asteria Health recalled 3,871 testosterone pellets on January 26, 2026, due to potential metal particulate matter. The recall affects products distributed nationwide in the USA. Consumers should stop using the product immediately and seek guidance from their healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
Read more
Food & Beverages
HIGH
FDA FOOD

Mangalm Tops GOLD Mixed Pickle Recalled for Erucic Acid Adulteration Risk (2026)

Mangalm LLC recalled Tops GOLD Mixed Pickle sold in California, Nevada, Oregon, Utah and Washington after FDA enforcement. The product may be adulterated with erucic acid from mustard oil. Consumers who purchased it should not eat it and should contact Mangalm for refund or replacement via email.

Mangalm
Potential adulteration
Read more
Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Screw System Recalled for MRI Heating Risk in 5,568 Units (2026)

I.T.S. GmbH has recalled 5,568 units of the I.T.S. Screw System sold nationwide in the United States after MRI safety tests showed higher RF-induced temperature increases under some MRI conditions than the IFU outlined. The defect involves MRI RF heating that could burn patients. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Recalled 510 I.T.S Straight Plate with Angular Stability Over MRI Heating Risk (2026)

ITS GmbH recalled 510 units of the I.T.S Straight Plate with Angular Stability after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The recall covers multiple article numbers across forearm and straight plates and distributions nationwide in the United States. No injuries or incidents have been reported at this time. Healthcare providers andpatients

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Pilon Plate with Angular Stability Recalled for MRI Heating Risk (2026) 101 Units

ITS GmbH recalls 101 Pilon Plate with Angular Stability implants distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than described in the IFU. Patients and healthcare providers should stop using the device immediately and follow recall instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS Fibula Plate PROlock with Angular Stability Recall Affects 869 Units (2026)

ITS recalls 869 Fibula Plate PROlock with Angular Stability implants distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than previously reflected in the IFU. Hospitals and healthcare providers should stop using this device immediately and follow the recall instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

I.T.S. GmbH Distal Humeral Plates Recalled for MRI Heating Risk — 12,059 Units (2026)

I.T.S. GmbH recalled 12,059 Distal Humeral Plates with Angular Stability due to MRI heating risk. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than reflected in the IFU. Healthcare providers and patients should stop using the device and follow recall instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Pelvic Reconstruction System Recall for MRI Heating Risk (46,637 Units) 2026

I.T.S. recalled 46,637 pelvic reconstruction system components nationwide in the United States after MRI safety testing showed higher RF-induced heating than the IFU stated. The issue centers on MRI heating under certain conditions that could injure patients. Patients should stop using the devices and follow manufacturer recall instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS Recalls 70 Olecranon Plates Over MRI RF Heating Risk (2026)

ITS recalls 70 Olecranon Plates with Angular Stability distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than described in the IFU. Patients and healthcare providers should stop using this device immediately and contact ITS or their healthcare provider for instructions.

I.T.S. GmbH
Updated MRI
Read more
Previous
12345...50
Next

Tag Statistics

Total Recalls
989

Related Tags

electrical hazardchemical hazardsuffocation riskinfant productchildren producttoddler productimmediate actionstop use immediatelyreturn for refundfda regulatedcpsc regulatedreplacement available